Dimethyl-benzoic acid compounds

ABSTRACT

The present invention provides a compound of the Formula II: 
     
       
         
         
             
             
         
       
         
         
           
             wherein A is: 
           
         
       
    
     
       
         
         
             
             
         
       
         
         
           
             R 1  is CH 3 , CF 3 , or F; 
             R 2  is H, CH 3 , or F; 
             R 3  is CH 3 , OCH 3 , OH, F; 
             R 4  is OH or CH 2 OH; and 
             X is CH or N; 
             or a pharmaceutically acceptable salt thereof.

The present invention relates to novel dimethyl-benzoic acid compounds,to pharmaceutical compositions comprising the compounds, to methods ofusing the compounds to treat physiological disorders, and tointermediates and processes useful in the synthesis of the compounds.

The present invention is in the field of treatment of inflammatoryconditions, such as arthritis, including osteoarthritis and rheumatoidarthritis, and further including pain associated with these conditions.Arthritis affects millions of patients in the United States alone and isa leading cause of disability. Treatments often include NSAIDs(nonsteroidal anti-inflammatory drugs) or COX-2 inhibitors, which mayproduce untoward cardiovascular side effects. As such, patients who havea poor cardiovascular profile, such as hypertension, may be precludedfrom using NSAIDs or COX-2 inhibitors. Thus, there is a need for analternative treatment of osteoarthritis and rheumatoid arthritis,preferably without the side effects of the current treatments.

Four prostaglandin E₂ (PGE₂) receptor subtypes have been identified asthe following: EP1, EP2, EP3 and EP4. It has been disclosed that EP4 isthe primary receptor involved in joint inflammatory pain in rodentmodels of rheumatoid arthritis and osteoarthritis (See J. Pharmacol.Exp. Ther., 325, 425 (2008)). Hence, a selective EP4 antagonist may beuseful in treating arthritis, including arthritic pain. In addition, ithas been suggested that since EP4 antagonism does not interfere withbiosynthesis of prostanoids, such as PGI₂ and TxA₂, a selective EP4antagonist may not possess the potential cardiovascular side effectsseen with NSAIDs and COX-2 inhibitors. (See for example Bioorganic &Medicinal Chemistry Letters, 21, 484 (2011)).

WO 96/02509 discloses certain quinoline derivatives which are selective,non-peptide NK3 antagonists useful in treating a variety of disordersincluding, for example, pulmonary disorders, CNS disorders, neurogenicinflammation, and inflammatory pain. In addition, U.S. Pat. No.7,705,035 discloses certain indoline amide derivatives useful as EP4ligands, agonists, or antagonists useful in treating various disorders,such as osteoarthritis, rheumatoid arthritis, and acute and chronicpain.

The present invention provides certain novel compounds that areselective inhibitors of EP4 relative to EP1, EP2, and EP3. In addition,the present invention provides certain novel compounds with thepotential for reduced cardiovascular or gastrointestinal side effects incomparison to traditional NSAIDs.

Accordingly, the present invention provides a compound of the FormulaII:

-   -   wherein A is:

-   -   R¹ is CH₃, CF₃, or F;    -   R² is H, CH₃, or F;    -   R³ is CH₃, OCH₃, OH, F;    -   R⁴ is OH or CH₂OH; and    -   X is CH or N;    -   or a pharmaceutically acceptable salt thereof.

The present invention further provides a compound of the Formula I:

or a pharmaceutically acceptable salt thereof.

The invention further provides a hydrated compound of Formula I.

The present invention also provides a method of treating arthritis in apatient, comprising administering to a patient in need of such treatmentan effective amount of a compound of Formula I or Formula II, or apharmaceutically acceptable salt thereof. The present invention alsoprovides a method of treating osteoarthritis in a patient, comprisingadministering to a patient in need of such treatment an effective amountof a compound of Formula I or Formula II, or a pharmaceuticallyacceptable salt thereof. In addition, the present invention provides amethod of treating rheumatoid arthritis in a patient, comprisingadministering to a patient in need of such treatment an effective amountof a compound of Formula I or Formula II, or a pharmaceuticallyacceptable salt thereof. The present invention also provides a method oftreating pain associated with arthritis in a patient, comprisingadministering to a patient in need of such treatment an effective amountof a compound of Formula I or Formula II, or a pharmaceuticallyacceptable salt thereof. The present invention further provides a methodof treating pain associated with osteoarthritis or rheumatoid arthritisin a patient, comprising administering to a patient in need of suchtreatment an effective amount of a compound of Formula I or Formula II,or a pharmaceutically acceptable salt thereof.

Furthermore, the invention provides a compound of Formula I or FormulaII, or a pharmaceutically acceptable salt thereof for use in therapy, inparticular for the treatment of osteoarthritis. In addition, theinvention provides a compound of Formula I or Formula II, or apharmaceutically acceptable salt thereof for use in the treatment ofrheumatoid arthritis. The invention also provides a compound of FormulaI or Formula II, or a pharmaceutically acceptable salt thereof for usein the treatment of pain associated with osteoarthritis or rheumatoidarthritis. Furthermore, the invention provides the use of a compound ofFormula I or Formula II, or a pharmaceutically acceptable salt thereof,for the manufacture of a medicament for the treatment of osteoarthritis.The invention provides the use of a compound of Formula I or Formula II,or a pharmaceutically acceptable salt thereof, for the manufacture of amedicament for the treatment of rheumatoid arthritis. The presentinvention also provides the use of a compound of Formula I or FormulaII, or a pharmaceutically acceptable salt thereof, for the manufactureof a medicament for the treatment of pain associated with osteoarthritisor rheumatoid arthritis.

The invention further provides a pharmaceutical composition comprising acompound of Formula I or Formula II, or a pharmaceutically acceptablesalt thereof, in combination with one or more pharmaceuticallyacceptable carriers, diluents, or excipients. In a particularembodiment, the composition further comprises one or more othertherapeutic agents. This invention also encompasses novel intermediatesand processes for the synthesis of the compound of Formula I or FormulaII, or a pharmaceutically acceptable salt thereof.

In addition, the invention includes a method of treating inflammatoryconditions such as arthritis, including osteoarthritis and rheumatoidarthritis, in a patient, comprising administering to a patient in needof such treatment an effective amount of an antagonist of aproinflammatory prostaglandin, such as an EP4 antagonist, in combinationwith an effective amount of a modulator of a lipoxin or resolvinreceptor, such as a modulator of BLT-1, BLT-2, ALX/FPR1, GPR32, CysLT1,CysLT2, or ChemR23.

A further aspect of the invention includes a method of treatinginflammatory disease such as arthritis, including osteoarthritis andrheumatoid arthritis, in a patient, comprising administering to apatient in need of such treatment an effective amount of an inhibitor ofa proinflammatory prostaglandin synthase, such as an mPGES-1 inhibitor,in combination with an effective amount of a modulator of a lipoxin orresolvin receptor, such as a modulator of BLT-1, BLT-2, ALX/FPR1, GPR32,CysLT1, CysLT2, or ChemR23.

As used herein, the terms “treating” or “to treat” includes restraining,slowing, stopping, or reversing the progression or severity of anexisting symptom or disorder.

As used herein, the term “patient” refers to a mammal, such as a mouse,guinea pig, rat, dog, or human. It is understood that the preferredpatient is a human.

As used herein, the term “effective amount” refers to the amount or doseof the compound of the invention, or a pharmaceutically acceptable saltthereof which, upon single or multiple dose administration to thepatient, provides the desired effect in the patient under diagnosis ortreatment.

An effective amount can be readily determined by the attendingdiagnostician, as one skilled in the art, by the use of known techniquesand by observing results obtained under analogous circumstances. Indetermining the effective amount for a patient, a number of factors areconsidered by the attending diagnostician, including, but not limitedto: the species of mammal; its size, age, and general health; thespecific disease or disorder involved; the degree of or involvement orthe severity of the disease or disorder; the response of the individualpatient; the particular compound administered; the mode ofadministration; the bioavailability characteristics of the preparationadministered; the dose regimen selected; the use of concomitantmedication; and other relevant circumstances.

The compound of Formula I or Formula II, or pharmaceutically acceptablesalt thereof, are generally effective over a wide dosage range. Forexample, dosages per day normally fall within the range of about 0.01 toabout 50 mg/kg of body weight. In some instances dosage levels below thelower limit of the aforesaid range may be more than adequate, while inother cases still larger doses may be employed with acceptable sideeffects, and therefore the above dosage range is not intended to limitthe scope of the invention in any way.

The compounds of the invention are preferably formulated aspharmaceutical compositions administered by any route which makes thecompound bioavailable. Most preferably, such compositions are for oraladministration. Such pharmaceutical compositions and processes forpreparing same are well known in the art. (See, e.g., Remington: TheScience and Practice of Pharmacy (D. B. Troy, Editor, 21 st Edition,Lippincott, Williams & Wilkins, 2006).

It is understood that Formula II includes Formula IIa and IIb:

The compounds of Formula I and Formula II are particularly useful in thetreatment methods of the invention, but certain groups, substituents,and configurations are preferred. The following paragraphs describe suchpreferred groups, substituents, and configurations. It will beunderstood that these preferences are applicable both to the treatmentmethods and to the new compounds of the invention.

It is preferred that A is:

It is preferred that R¹ is CH₃.

It is preferred that X is N.

It is further preferred that when R² is H, that R³ is OH.

A preferred compound is4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid, which is:

-   -   or a pharmaceutically acceptable salt thereof.

4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid is especially preferred.

Hydrated4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid is further preferred.

Hydrated4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid characterized by a substantial peak in the X-ray diffractionspectrum, at diffraction angle 2-theta, of 9.0°, in combination with twoor more peaks at diffraction angle 2-theta selected from the groupconsisting of 5.8°, 8.5°, 9.8°, 11.6°, 11.8°, 17.5°, and 24.2°, is alsopreferred.

As used herein, “DMEM” refers to Dulbecco's Modified Eagle's Medium;“DMSO” refers to dimethylsulfoxide; “IPA” refers to isopropyl alcohol;“MeOH” refers to methanol; “EtOH” refers to ethanol; “DMF” refers todimethylformamide; “THF” refers to tetrahydrofuran; “EtOAc” refers toethyl acetate; “FBS” refers to Fetal Bovine Serum; “PGE₂” refers toprostaglandin E₂; “FBS” refers to Fetal Bovine Serum; “IBMX” refers to(3-isobutyl-1-methylxanthine); “MES” refers to(2-(N-morpholino)ethanesulfonic acid; “HEPES” refers to(2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid); “HTRF” refersto homogeneous time-resolved fluorescence technology; “HEK” refers tohuman embryonic kidney; and “IC₅₀” refers to the concentration of anagent that produces 50% of the maximal inhibitory response possible forthat agent.

Pharmaceutically acceptable salts and common methodology for preparingthem are well known in the art. See, e.g., Gould, P. L., “Salt selectionfor basic drugs,” International Journal of Pharmaceutics, 33: 201-217(1986); Bastin, R. J., et al. “Salt Selection and OptimizationProcedures for Pharmaceutical New Chemical Entities,” Organic ProcessResearch and Development, 4: 427-435 (2000); and S. M. Berge, et al.,“Pharmaceutical Salts,” Journal of Pharmaceutical Sciences, 66: 1-19(1977). One skilled in the art of synthesis will appreciate that thecompound of Formula I is readily converted to and may be isolated aspharmaceutically acceptable salts using techniques and conditions wellknown to one of ordinary skill in the art.

The compounds of the present invention, or pharmaceutically acceptablesalts thereof, may be prepared by a variety of procedures known in theart, some of which are illustrated in the schemes, preparations, andexamples below. The specific synthetic steps for each of the routesdescribed may be combined in different ways, or in conjunction withsteps from different schemes, to prepare the compounds of Formula I orFormula II, or pharmaceutically acceptable salt thereof. The products ofeach step in the schemes below can be recovered by conventional methods,including extraction, evaporation, precipitation, chromatography,filtration, trituration, and crystallization. The reagents and startingmaterials are readily available to one of ordinary skill in the art. Allsubstituents, unless otherwise specified, are as previously defined. Itis understood that these schemes, preparations, and examples are notintended to be limiting to the scope of the invention in any way.

Preparation 1 Synthesis of 6-chloro-3-methyl-pyridine-2-carboxylic acid

Scheme 1, Step A.

A solution of aqueous 1N NaOH (10 ml) is added to a stirred solution ofmethyl 6-chloro-3-methyl-pyridine-2-carboxylate (1.0 g, 5.39 mmoles) inTHF:MeOH (10 ml:2 ml). The mixture is stirred at room temperature for 3hours. The organic solvent is removed under reduced pressure and thesemi-solid is dissolved in water and acidified to pH 1-2 with aqueous 1NHCl. The resulting precipitate is filtered, washed with water, and driedat 40° C. in a vacuum oven for 12 hours to give the title compound as awhite solid (780 mg, 84%). Mass spectrum (m/z): 172.0 (M+1).

Preparation 2 Synthesis of ethyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 1, Step B.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.78 g,4.55 mmol) in CH₂Cl₂ (15 mL) at room temperature are added ethyl4-amino-3,5-dimethyl-benzoate (0.878 g, 4.55 mmol) andN,N-diisopropylethylamine (1.98 ml, 11.36 mmol). After stirring thereaction mixture for 10 minutes, 1-propanephosphonic acid cyclicanhydride (50% solution in ethyl acetate, 3.25 ml, 5.46 mmol) is addedvia syringe. After 48 hours, the solvent is removed under reducedpressure and the residue is diluted with water and extracted with ethylacetate. The organic layers are combined and dried over magnesiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) usinga gradient of 0-40% ethyl acetate in hexanes. After purification, thesolid is triturated with 30% ethyl acetate in hexanes and filtered togive the title compound as a white powder (0.907 g, 57.5%). Massspectrum (m/z): 347.2 (M+1).

Preparation 3 Synthesis of tert-butyl-dimethyl-(4-piperidyloxy)silane

Scheme 1, Step C Reagent.

To a solution of 4-hydroxypiperidine (2.00 g, 9.89 mmoles) in CH₂Cl₂ (30mL) is added 1H-imidazole (2.69 g, 39.55 mmoles) followed byt-butyldimethylchlorosilane (3.58 g, 23.73 mmoles) and the reactionmixture is stirred at room temperature. After 12 hours, the reactionmixture is washed with water, saturated solution of NaHCO₃, and brine.The organic layers are combined and dried over sodium sulfate, filtered,and concentrated under reduced pressure. The resulting residue ispurified by flash chromatography (silica gel) over a gradient using 100%CH₂Cl₂ to 10% 7N ammonia in MeOH/90% CH₂Cl₂ to afford the title compound(3.69 g, 86.3%). Mass spectrum (m/z): 216.2 (M+1).

Preparation 4 Synthesis of ethyl4-[[6-[4-(tert-butyl(dimethyl)silyl)oxy-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 1, Step C.

To a solution of ethyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate,(440 mg, 1.27 mmol) in THF (1.6 mL) is added (iPr)Pd(cinnamyl)Cl (16.43mg, 0.03 mmol) followed by lithium bis(trimethylsilyl)amide (3.81 ml).The reaction mixture is purged with nitrogen for 5 minutes and thenstirred at room temperature. After 18 hours, the reaction is dilutedwith a saturated solution of NaHCO₃ and extracted with ethyl acetate.The organic layers are combined and dried over magnesium sulfate,filtered, and concentrated under reduced pressure. The resulting residueis purified by flash chromatography (silica gel) over a gradient using0-30% ethyl acetate in hexanes to afford the title compound (278 mg,41%). Mass spectrum (m/z): 526.2 (M+1).

Preparation 5 Synthesis of ethyl4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 1, Step D.

To a solution of ethyl4-[[6-[4-(tert-butyl(dimethyl)silyl)oxy-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(342 mg, 0.650 mmol) in THF (4 ml) is added Bu₄NF 1.0 M in THF (0.975ml, 0.975 mmol) at 0° C. The reaction mixture is gradually warmed toambient temperature. After 12 hours, the reaction mixture is dilutedwith ice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 0-40% ethyl acetate inhexanes to afford the title compound (223 mg, 83.3%). Mass spectrum(m/z): 412.2 (M+1).

Preparation 6 Synthesis of potassium6-chloro-3-methyl-pyridine-2-carboxylate

Scheme 2, Step A.

Methyl 6-chloro-3-methyl-pyridine-2-carboxylate (50 g, 269.4 mmoles) isadded to a solution of potassium hydroxide (18.7 g, 282.9 mmoles) inisopropyl alcohol (2000 mL). The mixture is stirred at ambienttemperature for 1 hour. Hexanes (500 mL) are added, and the solid isfiltered, washed with hexanes, and dried under reduced pressure at 45°C. for 4 hours to give the title compound (52 g, 92%). Mass spectrum(m/z): 172.0 (M+1). ¹H NMR (300 MHz, D₂O): 7.62 (d, J=8.0 Hz, 1H), 7.27(d, J=8.0 Hz, 1H), 2.23 (s, 3H).

Preparation 7 Synthesis of methyl4-[6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 2, Step B.

To a suspension of potassium 6-chloropyridine-2-carboxylate (52 g, 265.8mmoles) in dimethylformamide (676 mL) is addedbis(2-oxo-3-oxazolidinyl)phosphonic chloride (115 g, 451.8 mmoles). Themixture is stirred at ambient temperature for 30 minutes. Methyl4-amino-3,5-dimethyl-benzoate (42.9 g, 239.2 mmoles, see preparation 12)and diisopropylethylamine (115.9 mL, 664.5 mmoles) are added. Thereaction is stirred at ambient temperature for 16 hours. The mixture isthen poured into water (2000 mL) and is stirred for 30 minutes. Theresulting solid is filtered and dried under reduced pressure at 45° C.The dry material is triturated with hexane (1400 mL) over 2 hours. Thesolid is filtered and dried under vacuum to give the title compound (69g, 78%) as a white solid. Mass spectrum (m/z): 333.05 (M+1). ¹H NMR (300MHz, DMSO): 10.16 (s, 1H), 7.89 (d, J=8.2 Hz, 1H), 7.73 (s, 2H), 7.63(d, J=8.2 Hz, 1H), 3.85 (s, 3H), 2.49 (s, 3H), 2.28 (s, 6H).

Example 1 Synthesis of4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 3, Step A.

A solution of aqueous 1N NaOH (1.08 ml) is added to a stirred solutionof ethyl4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(223 mg, 0.541 mmol) in THF:MeOH (4 ml:2 ml). After heating at 40° C.for 12 hours, the organic solvent is removed under reduced pressure andthe semi-solid is dissolved in water and acidified to pH 3 with aqueous1N HCl. The resulting precipitate is filtered, washed with water, anddried at 40° C. in a vacuum oven for 12 hours to give the title compoundas a white solid (160 mg, 77%). Mass spectrum (m/z): 384.2 (M+1).

Alternative Synthesis of4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 3, Step B.

4-Hydroxypiperidine (171.2 g, 1660 mmoles) is added to a solution ofmethyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate(69 g, 207.3 mmoles) in N-methylpyrrolidone (483 mL) and the mixture isstirred at 150° C. for 4 hours. The mixture is cooled to ambienttemperature and poured into water (1000 mL). The mixture is washed withmethyl t-butyl ether (300 mL). The aqueous layer is then acidified to pH2 with aqueous 36% HCl. The mixture is extracted with a solution of 1/1ethyl acetate/methyl-t-butyl ether (3×250 mL). The organic layer isevaporated to dryness. Water (500 mL) is added to the residue and theresulting mixture is stirred for 30 minutes, filtered and the filteredmaterial dried in an oven vacuum at 45° C. overnight. The dried lightbrown solid is dissolved in acetone (500 mL) and heated to 50° C. Water(1000 mL) is slowly added and the mixture is stirred at 50° C. for 2hours. The mixture is cooled to ambient temperature, filtered, and thefiltered material dried under reduced pressure at 45° C. The driedmaterial is stirred in ethyl acetate (600 mL) at 50° C. for two hours.The mixture is cooled to ambient temperature, filtered, and the filteredmaterial dried under reduced pressure at 45° C. overnight to give thetitle compound as a white solid (50.8 g, 64%). Mass spectrum (m/z):384.2 (M+1). ¹H NMR (300 MHz, DMSO): 12.85 (s, 1H), 9.87 (s, 1H), 7.71(s, 2H), 7.49 (d, J=8.7 Hz, 1H), 7.01 (d, J=8.7 Hz, 1H), 4.68 (d, J=4.1Hz, 1H), 4.11-4.04 (m, 2H), 3.70 (m, 1H), 3.15-3.07 (m, 2H), 2.41 (s,3H), 2.27 (s, 6H), 1.81-1.77 (m, 2H), 1.44-1.32 (m, 2H).

X-Ray Powder Diffraction

The XRD patterns of crystalline solids are obtained on a Bruker D4Endeavor X-ray powder diffractometer, equipped with a CuKa source(λ=1.54060 Å) and a Vantec detector, operating at 35 kV and 50 mA. Thesample is scanned between 4 and 40° in 2θ, with a step size of 0.0087°in 2θ and a scan rate of 0.5 seconds/step, and with 0.6 mm divergence,5.28 mm fixed anti-scatter, and 9.5 mm detector slits. The dry powder ispacked on a quartz sample holder and a smooth surface is obtained usinga glass slide. It is well known in the crystallography art that, for anygiven crystal form, the relative intensities of the diffraction peaksmay vary due to preferred orientation resulting from factors such ascrystal morphology and habit. Where the effects of preferred orientationare present, peak intensities are altered, but the characteristic peakpositions of the polymorph are unchanged. See, e.g. The U.S.Pharmacopeia 35—National Formulary 30 Chapter <941> Characterization ofcrystalline and partially crystalline solids by X-ray powder diffraction(XRPD) Official Dec. 1, 2012-May 1, 2013. Furthermore, it is also wellknown in the crystallography art that for any given crystal form theangular peak positions may vary slightly. For example, peak positionscan shift due to a variation in the temperature or humidity at which asample is analyzed, sample displacement, or the presence or absence ofan internal standard. In the present case, a peak position variabilityof ±0.2 in 2θ will take into account these potential variations withouthindering the unequivocal identification of the indicated crystal form.Confirmation of a crystal form may be made based on any uniquecombination of distinguishing peaks (in units of ° 2θ), typically themore prominent peaks. The crystal form diffraction patterns, collectedat ambient temperature and relative humidity, were adjusted based onNIST 675 standard peaks at 8.85 and 26.77 degrees 2-theta.

Example A Preparation of hydrated4-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

4-[[6-(4-Hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid (240.7 mg) is dissolved in 10 ml of 1:1 acetone:water to give aclear pale solution. The mixture is concentrated at room temperature andcrystalline hydrated form begins to slowly precipitate from solutionover several minutes. The resulting solids are filtered and air dried togive 197.5 mg of the title compound.

A prepared sample of the title compound of Example A is characterized byan X-ray powder diffraction pattern using CuKa radiation as havingdiffraction peaks (2-theta values) as described in Table 1 below.Specifically the pattern contains a peak at 9.0° in combination with twoor more of the peaks selected from the group consisting of 5.8°, 8.5°,9.8°, 11.6°, 11.8°, 17.5°, and 24.2° with a tolerance for thediffraction angles of 0.2 degrees.

TABLE 1 X-ray powder diffraction peaks of Example A. Peak Angle (2-Theta°) Intensity (%) 1 5.8 43 2 8.5 16 3 9.0 100 4 9.8 21 5 11.6 62 6 11.834 7 14.1 9 8 15.3 15 9 15.4 30 10 17.5 43 11 20.4 11 12 20.8 21 13 22.713 14 24.2 35 15 24.6 19 16 27.5 9

Preparation 8 Synthesis of 1-iodo-2,4-dimethyl-3-nitro-benzene

Scheme 4, Step A:

To 1,3-dimethyl-2-nitro-benzene (68.5 g, 453.2 mmol) is added sulfuricacid (27.2 mL, 510 mmol), acetic acid (543.8 mL, 9.49 mol), iodine (46g, 181.3 mmol) and HIO₄ (91.9 g, 403.3 mmol). The reaction is heated to90° C. for 7 days. The reaction mixture is cooled to ambient temperatureand water (500 mL) is added. The resulting solid is collected byfiltration and washed with cold water. The solid is dried under reducedpressure at 45° C. overnight to afford the title compound as a yellowsolid (119 g, 95%). ¹H NMR (300.16 MHz, CDCl₃): δ 7.80 (d, J=8.2 Hz,1H), 6.85 (d, J=8.2 Hz, 1H), 2.37 (s, 3H), 2.23 (s, 3H).

Preparation 9 Synthesis of methyl 2,4-dimethyl-3-nitro-benzoate

Scheme 4, Step B:

To a 2 L Parr™ autoclave with mechanical stirring is added1-iodo-2,4-dimethyl-3-nitro-benzene (70 g, 252.7 mmol), Pd(OAc)₂ (2.8 g,12.6 mmol), 1,4-bis(diphenylphosphino)butane (6.5 g, 15.2 mmol),acetonitrile (462 mL), triethylamine (88.2 mL), and methanol (280 mL).The Parr™ autoclave is sealed, purged and pressurized with CO to 551.6kPa (80 psig). The mixture is heated to 100° C. for 2 hours. The mixtureis cooled to ambient temperature and then vented. The mixture is thenconcentrated to dryness under reduced pressure. Ethyl acetate (300 mL)and water (300 mL) are added. The layers are separated and the aqueouslayer discarded. The organic layer is dried over MgSO₄, filtered, andconcentrated to dryness to afford the title compound as a red oil whichcrystallizes upon standing (52 g, 98%). ¹H NMR (300.13 MHz, CDCl₃): δ7.89 (d, J=8.2 Hz, 1H), 7.19 (d, J=8.2 Hz, 1H), 3.91 (s, 3H), 2.49 (s,3H), 2.33 (s, 3H).

Preparation 10 Synthesis of methyl 3-amino-2,4-dimethyl-benzoate

Scheme 4, Step C:

To a solution of methyl 2,4-dimethyl-3-nitro-benzoate (37 g, 176.9 mmol)in methanol (370 mL), 10% palladium on carbon 50% wet (5.6 g) is added.The reaction is bubbled with hydrogen and placed under a hydrogenatmosphere for 6 days. The mixture is filtered through diatomaceousearth and the filtrate is evaporated to dryness. The resulting residueis purified by flash chromatography (silica gel), eluting with 20% ethylacetate in hexanes to afford the title compound as a yellow oil (20.5 g,65%). Mass spectrum (m/z): 180.1 (M+1). ¹H NMR (300.16 MHz, DMSO-d₆): δ6.89 (s, 2H), 4.78 (s, 2H), 3.76 (s, 3H), 2.23 (s, 3H), 2.12 (s, 3H).

Preparation 11 Synthesis of methyl 3,5-dimethyl-4-nitro-benzoate

Scheme 5, Step A.

To a solution of 3,5-dimethyl-4-nitro-benzoic acid (10.0 g, 0.0512 mol)in MeOH (150 mL) is added thionyl chloride (10 ml) at 0° C. and thereaction is heated to 80° C. After 16 h, the reaction mixture is cooledto room temperature and solvent is removed under reduced pressure. Theresidue is diluted with water (50 ml) and basified with saturated NaHCO₃solution to pH 7-8 and extracted with EtOAc (2×120 mL). The organiclayers are combined and dried over anhydrous sodium sulfate. The solventis removed under reduced pressure to afford the title compound as alight yellow solid (10.71 g, 98.3%). ¹H NMR (400 MHz, DMSO): δ 7.83 (s,2H), 3.88 (s, 3H), 2.30 (s, 6H).

Preparation 12 Synthesis of methyl 4-amino-3,5-dimethyl-benzoate

Scheme 5, Step B.

To a solution of methyl 3,5-dimethyl-4-nitrobenzoate (10.0 g, 0.0478mol) in methanol (100 mL), iron powder (15.7 g, 0.2869 mol) and 37% HCl(1.72 g, 0.0478 mol) is added at 0° C. The reaction is heated at 80° C.for 16 hours. The mixture is cooled to room temperature and filteredthrough Celite™ bed and washed with methanol followed by evaporation offiltrate to dryness to afford the title compound as a brown solid (7.8g, 99%). Mass spectrum (m/z): 180.2 (M+1).

Preparation 13 Synthesis of methyl4-[(5-bromo-2-fluoro-benzoyl)amino]-3,5-dimethyl-benzoate

Scheme 6, Step A.

To a solution of 5-bromo-2-fluorobenzoic acid (3.50 g, 15.9 mmol) inCH₂Cl₂ (50 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate(2.86 g, 15.9 mmol, see preparation 12) and N,N-diisopropylethylamine(8.35 ml, 47.9 mmol). After stirring the reaction mixture for 10minutes, 1-propanephosphonic acid cyclic anhydride (50% solution inethyl acetate, 20.5 ml, 31.9 mmol) is added via syringe and stirred atambient temperature. After 36 hours, the solvent is removed underreduced pressure and the residue is diluted with water and extractedwith ethyl acetate. The organic layers are combined and dried overanhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) using10% ethyl acetate in hexane to give the title compound as a white solid(4.20 g, 69%). Mass spectrum (m/z): 380.2 (M+1).

Preparation 14 Synthesis oftert-butyl-dimethyl-(3-piperidylmethoxy)silane

Scheme 6, Step B.

To a solution of piperidin-3-ylmethanol (2.10 g, 0.018 mol) in CH₂Cl₂(20 mL) is added triethylamine (5.53 g, 0.0547 mol) followed byt-butyldimethylchlorosilane (4.127 g, 0.0275 mol) and the reactionmixture is stirred at room temperature. After 24 hours, the reactionmixture is washed with water, saturated solution of NaHCO₃, and brine.The combined organic layers are combined and dried over sodium sulfate,filtered, and concentrated under reduced pressure. The resulting residueis purified by flash chromatography (silica gel) over a gradient using0-10% MeOH in dichloromethane to afford the title compound (2.50 g,60%). Mass spectrum (m/z): 231.2 (M+1).

Preparation 15 Synthesis of methyl4-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-fluoro-benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 6, Step B.

To a solution of methyl4-[(5-bromo-2-fluoro-benzoyl)amino]-3,5-dimethyl-benzoate (0.40 g, 1.05mmol), tert-butyl-dimethyl-(3-piperidylmethoxy)silane (0.362 g, 1.57mmol) and Cs₂CO₃ (1.04 g, 3.15 mmol) in 1,4-dioxane (6 ml) is addedPd₂(dba)₃ (0.10 g, 0.105 mmol) followed by S-Phos (0.043 g, 0.105 mmol).The reaction mixture is purged with nitrogen for 5 minutes and thenheated at 90° C. After 16 hours, the reaction is cooled to ambienttemperature, filtered through Celite™, and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure and purified by flash chromatography(silica gel) using 10% EtOAc in hexane to afford the title compound as apale yellow oil (0.22 g, 40%). Mass spectrum (m/z): 529.2 (M+1).

Preparation 16 Synthesis of methyl4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino-]-3,5-dimethyl-benzoate

Scheme 6, Step C.

To a solution of methyl4-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-fluoro-benzoyl]amino]-3,5-dimethyl-benzoate(0.30 g, 0.54 mmol) in THF (8 ml) is added Bu₄NF 1.0 M in THF (0.35 g,1.60 mmol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 4 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using ethyl acetate inhexanes as eluent to afford the title compound as a white solid (0.10 g,55%). Mass spectrum (m/z): 414.2 (M+1).

Example 2 Synthesis of4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoicacid

Scheme 6, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof methyl4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoate(0.18 g, 0.43 mmol) in THF:MeOH (3 ml:1 ml). After 16 h at 50° C., theorganic solvent is removed under reduced pressure and the residue isdiluted with water, acidified to pH 4 with 1N HCl and extracted withCH₂Cl₂. The organic layers are combined and dried over anhydrous sodiumsulfate. The solvent is removed under reduced pressure and the resultingprecipitate is triturated with diethyl ether and filtered to afford thetitle compound as a white solid (0.12 g, 69%). Mass spectrum (m/z):401.2 (M+1).

Chiral separation of racemic4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoicacid

4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoicacid is separated by chiral chromatography using Chiralpak™ AD-H, 25%MeOH/CO2, 5 ml/min, 225 nm to give:

Example 2A

4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoicacid isomer 1. Peak eluting at 2.52 min Mass spectrum (m/z): 401.2(M+1).

Example 2B

4-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-3,5-dimethyl-benzoicacid isomer 2. Peak eluting at 2.93 min Mass spectrum (m/z): 401.2(M+1).

Preparation 17 Synthesis of methyl3-[(5-bromo-2-fluoro-benzoyl)amino]-2,4-dimethyl-benzoate

Scheme 7, Step A.

To a solution of 5-bromo-2-fluoro-benzoic acid (500 mg, 2.28 mmol) inCH₂Cl₂ (15 mL) at 0° C. are added methyl 3-amino-2,4-dimethylbenzoate(409 mg, 2.28 mmol, see preparation 10) and N,N-diisopropylethylamine(737.6 mg, 5.71 mmol). After stirring the reaction mixture for 10minutes, 1-propanephosphonic acid cyclic anhydride (50% solution inethyl acetate, 1.74 g, 2.74 mmol) is added via syringe and stirred at50° C. After 16 hours, the solvent is removed under reduced pressure andthe residue is triturated with MeOH to give the title compound as awhite solid (450 mg, 51.8%). Mass spectrum (m/z): 380.2 (M+1).

Preparation 18 Synthesis of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-fluoro-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 7, Step B.

To a solution of methyl3-[(5-bromo-2-fluoro-benzoyl)amino]-2,4-dimethyl-benzoate (0.7 g, 1.84mmol), tert-butyl-dimethyl-(3-piperidylmethoxy)silane (2.53 g, 11.03mmol, see preparation 14) and Cs₂CO₃ (1.81 g, 5.50 mmol) in 1,4-dioxane(15 ml) is added Pd₂(dba)₃ (0.168 g, 0.184 mol) followed by S-Phos(0.075 g, 0.184 mol). The reaction mixture is purged with nitrogen for 5minutes and then heated at 120° C. After 6 hours, the reaction mixtureis concentrated under reduced pressure and residue is carried forwardwithout further purification.

Preparation 19 Synthesis of methyl3-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 7, Step C.

To a solution of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-fluoro-benzoyl]amino]-2,4-dimethyl-benzoate(2.9 g, 5.48 mmol) in THF (20 ml) is added Bu₄NF 1.0 M in THF (5.73 g,0.0219 mol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 4 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 35-45% ethyl acetatein hexane to afford the title compound as a white solid (0.38 g, 16.8%).Mass spectrum (m/z): 415.2 (M+1).

Example 3 Synthesis of3-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 7, Step D.

A solution of NaOH (0.146 mg, 0.00366 mol) in 1.5 ml of H₂O is added toa stirred solution of methyl3-[[2-fluoro-5-[3-(hydroxymethyl)-1-piperidyl]benzoyl]amino]-2,4-dimethyl-benzoate(0.38 g, 0.000916 mol) in THF:EtOH (3 ml:2 ml). After 4 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted with ethyl acetate. The organic layer are combined and driedover anhydrous sodium sulfate. The solvent is removed under reducedpressure to afford the title compound as a light yellow solid (85 mg g,36.8%). Mass spectrum (m/z): 401.2 (M+1).

Preparation 20 Synthesis of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate

Scheme 8, Step A.

To a solution of 5-bromo-2-methylbenzoic acid (2.0 g, 0.0093 mol) inCH₂Cl₂ (20 mL) at 0° C. are added methyl 3-amino-2,4-dimethylbenzoate(1.49 g, 0.0084 mol, see preparation 10) and N,N-diisopropylethylamine(4.79 g, 0.0372 mol). After stirring the reaction mixture for 10minutes, 1-propanephosphonic acid cyclic anhydride (50% solution inethyl acetate, 8.87 g, 0.028 mol) is added via syringe and stirred at50° C. After 16 hours, the solvent is removed under reduced pressure andthe residue is diluted with water and extracted twice with ethylacetate. The organic layers are combined and dried over anhydrousNa₂SO₄, filtered, and concentrated under reduced pressure. The resultingresidue is purified by flash chromatography (silica gel) using 10% ethylacetate in hexane to give the title compound as a white solid (2.80 g,80%). Mass spectrum (m/z): 376.1 (M+1).

Preparation 21 Synthesis of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 8, Step B.

To a solution of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate (0.5 g, 1.32mmol), tert-butyl-dimethyl-(3-piperidylmethoxy)silane (0.45 g, 1.99mmol, see preparation 14) and Cs₂CO₃ (1.29 g, 3.98 mmol) in 1,4-dioxane(15 ml) is added Pd₂(dba)₃ (0.12 g, 0.132 mmol) followed by S-Phos(0.050 g, 0.132 mmol). The reaction mixture is purged with nitrogen for5 minutes and then heated at 110° C. After 6 hours, the reaction iscooled to ambient temperature, filtered through Celite™, and washed withEtOAc. The combined filtrates are dried over sodium sulfate, filtered,and concentrated under reduced pressure and purified by flashchromatography (silica gel) using 15% EtOAc in hexane as eluent toafford the title compound as a brown semi solid (0.6 g, 85%). Massspectrum (m/z): 525.2 (M+1).

Preparation 22 Synthesis of methyl3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 8, Step C.

To a solution of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.60 g, 1.14 mmol) in THF (15 ml) is added Bu₄NF 1.0 M in THF (0.596 g,2.28 mmol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 1 hour, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 4% methanol indichloromethane as eluent to afford the title compound as a white solid(0.4 g, 85.5%). Mass spectrum (m/z): 411.4 (M+1).

Example 4 Synthesis of3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 8, Step D.

A solution of aqueous 4N NaOH (4.00 ml) is added to a stirred solutionof methyl3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.4 g, 0.975 mmol) in THF:MeOH (10 ml:5 ml). After 4 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted twice with 10% IPA in CH₂Cl₂. The organic layers are combinedand dried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as a light brownsolid (0.28 g, 72.5%). Mass spectrum (m/z): 397.2 (M+1).

Chiral separation of racemic3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid

3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid is separated by chiral chromatography using Chiralcel™ OJ-H, 15%MeOH/CO2, 5 ml/min, 225 nm to give:

Example 4A

3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid isomer 1. Peak eluting at 1.76 min Mass spectrum (m/z): 397.2(M+1).

Example 4B

3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid isomer 2. Peak eluting at 2.49 min Mass spectrum (m/z): 397.2(M+1).

Preparation 23 Synthesis of methyl4-[(5-bromo-2-methyl-benzoyl)amino]-3,5-dimethyl-benzoate

Scheme 9, Step A.

To a solution of 5-bromo-2-methylbenzoic acid (2.0 g, 0.008 mol) inCH₂Cl₂ (20 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate(1.28 g, 0.0072, see preparation 12) and N,N-diisopropylethylamine (4.12g, 0.032 mol). After stirring the reaction mixture for 10 minutes,1-propanephosphonic acid cyclic anhydride (50% solution in ethylacetate, 7.63 g, 0.024 mol) is added via syringe and stirred at 50° C.After 16 hours, the solvent is removed under reduced pressure and theresidue is diluted with water and extracted twice with ethyl acetate.The organic layers are combined and dried over anhydrous Na₂SO₄,filtered, and concentrated under reduced pressure. The resulting residueis purified by flash chromatography (silica gel) using 12% ethyl acetatein hexane to give the title compound as a white solid (2.9 g, 97%). Massspectrum (m/z): 376.0 (M+1).

Preparation 24 Synthesis of methyl4-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 9, Step B.

To a solution of methyl4-(5-bromo-2-methylbenzamido)-3,5-dimethylbenzoate (0.5 g, 0.0013 mol),tert-butyl-dimethyl-(3-piperidylmethoxy)silane (0.45 g, 0.0019 mol,preparation 14) and Cs₂CO₃ (1.29 g, 0.0039 mol) in 1,4-dioxane (15 ml)is added Pd₂(dba)₃ (0.12 g, 0.00013 mol) followed by S-Phos (0.054 g,0.00013 mol). The reaction mixture is purged with nitrogen for 5 minutesand then heated at 110° C. After 16 hours, the reaction is cooled toambient temperature, filtered through Celite™ and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure and purified by flash chromatography(silica gel) using 15% ethyl acetate in hexane as eluent to afford thetitle compound as a brown semi solid (0.4 g, 57.3%). Mass spectrum(m/z): 525.2 (M+1).

Preparation 25 Synthesis of methyl4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 9, Step C.

To a solution of methyl4-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate(0.40 g, 0.76 mmol) in THF (10 ml) is added Bu₄NF 1.0 M in THF (0.39 g,1.52 mmol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 1 hour, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 4% MeOH indichloromethane to afford the title compound as a light brown solid(0.30 g, 96%). Mass spectrum (m/z): 411.5 (M+1).

Example 5 Synthesis of4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid

Scheme 9, Step D.

A solution of aqueous 4N NaOH (2.00 ml) is added to a stirred solutionof methyl4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate(0.3 g, 0.73 mmol) in THF:MeOH (10 ml:5 ml). After 16 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted with 10% IPA in CH₂Cl₂. The organic layers are combined anddried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as a light brownsolid (0.27 g, 90%). Mass spectrum (m/z): 397.2 (M+1).

Chiral separation of racemic4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid

4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid is separated by chiral chromatography using Chiralpak AD-H, 30%EtOH/CO₂, 5 ml/min, 225 nm to give:

Example 5A

4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid isomer 1. Peak eluting at 4.22 min Mass spectrum (m/z): 397.2(M+1).

Example 5B

4-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid isomer 2. Peak eluting at 5.30 min Mass spectrum (m/z): 397.2(M+1).

Preparation 26 Synthesis of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]pyrrolidin-1-yl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 10, Step A.

To a solution of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate (0.5 g, 1.32mmol), tert-butyl-dimethyl-(pyrrolidin-3-ylmethoxy)silane (0.4 g, 1.99mmol) and Cs₂CO₃ (1.2 g, 3.99 mmol) in 1,4-dioxane (15 ml) is addedPd₂(dba)₃ (0.12 g, 0.132 mmol) followed by S-Phos (0.054 g, 0.132 mmol).The reaction mixture is purged with nitrogen for 5 minutes and thenheated at 100° C. After 16 hours, the reaction is cooled to ambienttemperature, filtered through Celite™, and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure and purified by flash chromatography(silica gel) using 20% EtOAc in hexane to afford the title compound as abrown semi solid (0.36 g, 53%). Mass spectrum (m/z): 511.2 (M+1).

Preparation 27 Synthesis of methyl3-[[5-[3-(hydroxymethyl)pyrrolidin-1-yl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 10, Step B.

To a solution of methyl3-[[5-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]pyrrolidin-1-yl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.35 g, 0.686 mmol) in THF (50 ml) is added Bu₄NF 1.0 M in THF (0.537g, 2.05 mmol) at 0° C. The reaction mixture is gradually warmed toambient temperature. After 2 hours, the reaction mixture is diluted withice-water and extracted twice with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 50% ethyl acetate inhexane to afford the title compound as a brown solid (150 mg, 51%).

Example 6 Synthesis of3-[[5-[3-(hydroxymethyl)pyrrolidin-1-yl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 10, Step C.

A solution of aqueous 5N NaOH (5.00 ml) is added to a stirred solutionof methyl3-[[5-[3-(hydroxymethyl)-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.4 g, 0.975 mmol) in MeOH (5 ml). After 5 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted twice with 10% IPA in CH₂Cl₂. The organic layers are combinedand dried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as a brown solid(70 mg, 56%). Mass spectrum (m/z): 381.2 (M−1).

Preparation 28 Synthesis of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate

Scheme 11, Step A.

To a solution of 5-bromo-2-methyl-benzoic acid (2.0 g, 0.0093 mol) inCH₂Cl₂ (20 ml) at room temperature are added methyl3-amino-3,5-dimethylbenzoate (1.49 g, 0.0083 mol, see preparation 12)and N,N-diisopropylethylamine (4.79 g, 0.037 mol). After stirring thereaction mixture for 10 minutes, 1-propanephosphonic acid cyclicanhydride (50% solution in ethyl acetate, 8.87 g, 0.027 mol) is addedvia syringe and heated at 50° C. After 16 hours, the reaction mixture isdiluted with CH₂Cl₂, washed with water and brine. The organic layers arecombined and dried over anhydrous Na₂SO₄, filtered, and concentratedunder reduced pressure. The residue is purified by flash chromatography(silica gel) using 10% EtOAc in hexanes to give the title compound as awhite powder (2.8 g, 80%).

Preparation 29 Synthesis of methyl3-[[5-[3-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 11, Step B.

To a solution of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate (0.5 g, 1.32mmol), tert-butyl-dimethyl-(3-piperidyloxy)silane (0.425 g, 1.98 mmol)and Cs₂CO₃ (1.28 g, 3.96 mmol) in 1,4-dioxane (15 ml) is added Pd₂(dba)₃(0.12 g, 0.132 mmol) followed by S-Phos (0.054 g, 0.132 mmol). Thereaction mixture is purged with nitrogen for 5 minutes and then heatedat 100° C. After 16 hours, the reaction is cooled to ambienttemperature, filtered through Celite™, and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure and purified by flash chromatography(silica gel) using 10% EtOAc in hexane to afford the title compound as abrown semi-solid (0.4 g, 60%).

Preparation 30 Synthesis of methyl3-[[5-(3-hydroxy-1-piperidyl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 11, Step C.

To a solution of methyl3-[[5-[3-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.4 g, 0.78 mmol) in THF (20 ml) is added Bu₄NF 1.0 M in THF (0.409 g,1.56 mmol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 1 hour, the reaction mixture is diluted withice-water and extracted twice with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 3% methanol indichloromethane to afford the title compound as a white solid (0.3 g,97%).

Example 7 Synthesis of3-[[5-(3-hydroxy-1-piperidyl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 11, Step D.

A solution of aqueous 4N NaOH (2.00 ml) is added to a stirred solutionof methyl3-[[5-(3-hydroxy-1-piperidyl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(0.3 g, 0.75 mmol) in THF:MeOH (5 ml:2 ml). After 3 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted with 10% IPA in CH₂Cl₂. The organic layers are combined anddried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as an off-whitesolid (0.274 g, 94%). Mass spectrum (m/z): 383.2 (M+1).

Preparation 31 Synthesis of ethyl4-[(5-bromo-2-methyl-benzoyl)amino]-3,5-dimethyl-benzoate

Scheme 12, Step A.

To a solution of 5-bromo-2-methyl-benzoic acid (1.35 g, 6.15 mmol) inTHF (15 ml), CH₂Cl₂ (15 ml) and DMF (14.27 μl, 184.57 μmoles) is addeddropwise oxalyl chloride (587.12 μl, 6.77 mmoles) at 0° C. and reactionmixture is slowly allowed to warm to ambient temperature. After 2 hours,the solvent is removed under reduced pressure. To the residue CH₂Cl₂ (30ml) is added and reaction mixture is cooled to 0° C., then ethyl4-amino-3,5-dimethyl-benzoate (1.19 g, 6.15 mmol) is added followed by4-pyridinamine, N,N-dimethyl-(37.58 mg, 307.61 μmoles) and pyridine(1.49 ml, 18.46 mmoles). The cooling bath is removed and the clearsolution is allowed to warm to ambient temperature. After 5 hours, thesolvent is removed and the reaction mixture is diluted with ethylacetate and washed with 1N HCl, saturated solution of sodiumbicarbonate, and brine. The organic layers are combined and dried overanhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. Theresulting residue is triturated with hexanes and the resulting solidswere collected by filtration to give the title compound as a white solid(1.80 g; 75.2%). Mass spectrum (m/z): 390.2 (M+1).

Preparation 32 Synthesis of ethyl4-[[5-(1,4-dioxa-8-azaspiro[4.51]decan-8-yl)-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 12, Step B.

To a solution of ethyl4-[(5-bromo-2-methyl-benzoyl)amino]-3,5-dimethyl-benzoate (0.5 g, 1.28mmol), 1,4-dioxa-8-azaspiro(4.5)decane (0.22 g, 1.54 mmol) and Cs₂CO₃(1.25 g, 3.84 mmol) in THF (10 ml) is added Pd(OAc)₂ (0.04 g, 0.19 mmol)followed by racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (119.7mg, 0.19 mmol). The reaction mixture is purged with nitrogen for 5minutes and then heated at 90° C. After 16 hours, the reaction is cooledto ambient temperature and diluted with ammonium chloride and extractedtwice with EtOAc. The combined organic layers are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) using0-100% ethyl acetate in hexane to afford the title compound as a brownsolid (0.21 g, 36.2%). Mass spectrum (m/z): 453.2 (M+1).

Preparation 33 Synthesis of ethyl3,5-dimethyl-4-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoate

Scheme 12, Step C.

To a solution of ethyl4-[[5-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoate(205 mg, 452.99 μmoles) in acetone (5 ml) is added a mixture of 5M HCl(1 mL) in H₂O (1 mL) and heated to 60° C. After 12 hours, the mixture iscooled to ambient temperature, diluted with 2M NaOH to pH 6 andextracted with ethyl acetate. The combined organic layers are dried oversodium sulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) using0-40% ethyl acetate in hexane to afford the title compound as anoff-white foam (0.11 g, 61%). Mass spectrum (m/z): 409.2 (M+1).

Preparation 34 Synthesis of3,5-dimethyl-4-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoicacid

Scheme 12, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof ethyl3,5-dimethyl-4-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoate(0.11 g, 269.28 μmol) in THF:MeOH (2.4 ml:1.2 ml). After 16 hours atambient temperature, the organic solvent is removed under reducedpressure and the residue is diluted with water, acidified to pH 7 with1N HCl, and extracted twice with ethyl acetate. The organic layers arecombined with aqueous layer and concentrated under reduced pressure. Theresulting solids are triturated with 1:1 mixture of acetonitrile andethanol to give white slurry that is filtered through Celite™ bed. Thefiltrate is concentrated under reduced pressure and the precipitate istriturated with acetone and filtered to afford the title compound as anoff-white solid (99 mg, 99%). Mass spectrum (m/z): 381.2 (M+1).

Example 8 Synthesis of4-[[5-(4-hydroxy-1-piperidyl)-2-methyl-benzoyl]amino]-3,5-dimethyl-benzoicacid

Scheme 12, Step E.

To a solution of3,5-dimethyl-4-[[2-methyl-5-(4-oxo-1-piperidyl)-benzoyl]amino]benzoicacid (69.5 mg, 182.68 μmoles) in methanol (1.83 ml) is added sodiumtetrahydroborate (13.82 mg, 365.36 μmoles) and the resulting mixture isstirred at ambient temperature. After 1 hour, the mixture is quenchedwith saturated solution of NH₄Cl (0.2 ml) and extracted with CHCl₃ (3ml):IPA (1 ml). The combined organic layers are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. Theresulting solid is triturated with H₂O (5 ml), filtered, and washed withH₂O (5 ml). The residue is purified by reverse phase chromatography(C18) using 20% acetonitrile in H₂O with 0.1% formic acid to afford thetitle compound as a white powder (0.01 g, 15.7%). Mass spectrum (m/z):383.2 (M+1).

Preparation 35 Synthesis of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate

Scheme 13, Step A.

To a solution of 5-bromo-2-methyl-benzoic acid (2.45 g, 11.16 mmol) inTHF (10 ml), CH₂Cl₂ (10 ml) and DMF (20.00 μl, 258.65 μmoles) is addeddropwise oxalyl chloride (1.16 ml, 13.39 mmoles) at 0° C. and thereaction mixture is slowly allowed to warm to ambient temperature. After2 hours, the solvent is removed under reduced pressure. To the residueis added CH₂Cl₂ (40 ml) and the reaction mixture is cooled to 0° C.,then ethyl 4-amino-3,5-dimethyl-benzoate (2 g, 11.16 mmol) is addedfollowed by N,N-dimethylpyridin-4-amine (13.63 mg, 0.11 mmoles) andpyridine (2.71 ml, 33.48 mmoles). The cooling bath is removed and theclear solution is allowed to warm to ambient temperature. After 2 hours,the solvent is removed and the reaction mixture is diluted with ethylacetate and washed with 1N HCl, a saturated solution of sodiumbicarbonate, and brine. The organic layers are combined, dried overanhydrous Na₂SO₄, filtered, and concentrated under reduced pressure togive the title compound as a light yellow solid (4.0 g; 95.5%). Massspectrum (m/z): 376.0 (M+1).

Preparation 36 Synthesis of methyl3-[[5-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 13, Step B.

To a solution of methyl3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate (0.5 g, 1.33mmol), 1,4-dioxa-8-azaspiro(4.5)decane (228.34 mg, 1.59 mmol) and Cs₂CO₃(1.3 g, 3.99 mmol) in 1,4-dioxane (10 ml) is added Pd(OAc)₂ (29.84 mg,132.89 μmol) followed byracemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (82.75 mg, 132.89μmol). The reaction mixture is purged with nitrogen for 10 minutes andthen heated to 90° C. After 3 hours, very small amount of the product isformed. To the reaction mixture is added Pd(OAc)₂ (29.84 mg, 132.89μmol) followed by racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl(82.75 mg, 132.89 μmol) and heated to 100° C. After 12 hours, thereaction is cooled to ambient temperature and diluted with water andextracted with EtOAc. The combined organic layers are washed with brine,dried over sodium sulfate, filtered, and concentrated under reducedpressure. The resulting residue is purified by flash chromatography(silica gel) using 0-100% ethyl acetate in hexane to afford the titlecompound as a brown solid (0.26 g, 44.62%). Mass spectrum (m/z): 439.2(M+1).

Preparation 37 Synthesis of methyl2,4-dimethyl-3-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoate

Scheme 13, Step C.

To a solution of methyl3-[[5-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoate(250 mg, 570.09 μmoles) in THF (2 ml) is added 4M HCl (1 ml) and stirredat ambient temperature. The mixture is concentrated under reducedpressure and re-dissolved in acetone (5 ml) followed by the addition of5N HCl (1 ml). After 22 hours at 60° C., the mixture is cooled toambient temperature and diluted with 2M NaOH to pH 6 and extracted twicewith ethyl acetate. The combined organic layers are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) using0-50% ethyl acetate in hexane to afford the title compound as anoff-white foam (0.12 g, 53.36%). Mass spectrum (m/z): 395.2 (M+1).

Preparation 38 Synthesis of2,4-dimethyl-3-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoicacid

Scheme 13, Step D.

A solution of aqueous 2N NaOH (1.00 ml) is added to a stirred solutionof methyl2,4-dimethyl-3-[[2-methyl-5-(4-oxo-1-piperidyl)benzoyl]amino]benzoate(0.12 g, 304.20 μmol) in THF:MeOH (2 ml:1 ml). After 16 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 6 with 1N HCl, andextracted with ethyl acetate. The organic layers are combined withaqueous layer and concentrated under reduced pressure. The resultingsolids are dissolved in acetonitrile/H₂O and lyophilized to afford thetitle compound as an off-white solid (58 mg, 50.12%). Mass spectrum(m/z): 381.2 (M+1).

Example 9 Synthesis of3-[[5-(4-hydroxy-1-piperidyl)-2-methyl-benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 13, Step E.

To a solution of2,4-dimethyl-3-[[2-methyl-5-(4-oxo-1-piperidyl)-benzoyl]amino]benzoicacid (51 mg, 134.05 μmoles) in methanol (1.34 ml) is added sodiumtetrahydroborate (10.14 mg, 268.11 μmoles) and the mixture is stirred atambient temperature. After 1 hour, the mixture is quenched and adjustedto pH7 with saturated solution of NH₄Cl and extracted twice with CHCl₃(3 ml):IPA (1 ml). The combined organic layers are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. The solid isre-dissolved in 3:1 CHCl₃:IPA and diluted with HCl to pH2 and extractedwith 3:1 CHCl₃:IPA. The combined organic layers are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is taken up in MeOH and filtered through cotton plug.The filtrate is concentrated under reduced pressure followed bydissolution in H₂O and lyophilized for 12 hours to afford the titlecompound as an off-white powder (0.04 g, 81.9%). Mass spectrum (m/z):383.2 (M+1).

Preparation 39 Synthesis of 6-chloro-3-methyl-pyridine-2-carboxylic acid

Scheme 14, Step A.

A solution of aqueous 1N NaOH (10.00 ml) is added to a stirred solutionof methyl 6-chloro-3-methyl-pyridine-2-carboxylate (1.0 g, 5.39 mmoles)in THF:MeOH (10 ml:2 ml). The mixture is stirred at room temperature for3 hours. The organic solvent is removed under reduced pressure and thesemi-solid is dissolved in water and acidified to pH 1-2 with aqueous 1NHCl. The resulting precipitate is filtered, washed with water, and driedat 40° C. in vacuum oven for 12 hours to give the title compound as awhite solid (780 mg, 84%). Mass spectrum (m/z): 172.0 (M+1).

Preparation 40 Synthesis of methyl3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoate

Scheme 14, Step B.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.35 g,0.20 mmol) in CH₂Cl₂ (6 ml) at room temperature are added methyl3-amino-3,5-dimethylbenzoate (0.36 g, 0.20 mmol, see preparation 12),and N,N-diisopropylethylamine (0.77 g, 0.60 mmol). After stirring thereaction mixture for 10 minutes, 1-propanephosphonic acid cyclicanhydride (50% solution in ethyl acetate, 2.54 g, 0.80 mmol) is addedvia syringe. After 16 hours at ambient temperature, the reaction mixtureis diluted with CH₂Cl₂, washed with water and brine. The organic layersare combined and dried over anhydrous Na₂SO₄, filtered, and concentratedunder reduced pressure to give the title compound as a white powder(0.52 g, 76%). Mass spectrum (m/z): 333.2 (M+1).

Preparation 41 Synthesis of tert-butyl-dimethyl-(4-piperidyloxy)silane

Scheme 14, Step C.

To a solution of 4-hydroxypiperidine (2.00 g, 9.89 mmoles) in CH₂Cl₂ (30mL) is added 1H-imidazole (2.69 g, 39.55 mmoles) followed byt-butyldimethylchlorosilane (3.58 g, 23.73 mmoles) and the reactionmixture is stirred at room temperature. After 12 hours, the reactionmixture is washed with water, saturated solution of NaHCO₃, and brine.The organic layers are combined and dried over sodium sulfate, filtered,and concentrated under reduced pressure. The resulting residue ispurified by flash chromatography (silica gel) over a gradient using 100%CH₂Cl₂ to 10% 7N ammonia in MeOH/90% CH₂Cl₂ to afford the title compound(3.69 g, 86.3%). Mass spectrum (m/z): 216.2 (M+1).

Preparation 42 Synthesis of methyl3-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 14, Step C.

To a solution of methyl3-(6-chloro-3-methylpicolinamido)-2,4-dimethylbenzoate (0.50 g, 0.0015mol), tert-butyl-dimethyl-(4-piperidyloxy)silane (0.90 g, 0.0045 mol)and Cs₂CO₃ (2.00 g, 0.006 mol) in toluene (6 ml) is added Pd₂(dba)₃(0.14 g, 0.00015 mol) followed by BINAP (0.086 g, 0.00015 mol). Thereaction mixture is purged with nitrogen for 5 minutes and then heatedat 120° C. After 4 hours, the reaction is cooled to ambient temperature,filtered through Celite™, and washed with EtOAc. The combined filtrateis dried over sodium sulfate, filtered, and concentrated under reducedpressure to afford the title compound as a white semi-solid (0.220 g,29%). Mass spectrum (m/z): 398.2 (M+1).

Example 10 Synthesis of3-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoicacid

Scheme 14, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof methyl3-[[6-(4-hydroxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate(0.21 g, 0.52 mmol) in THF:MeOH (3 ml:1 ml). After 16 h at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 6 with aqueous 1NHCl, and extracted with ethyl acetate (2×20 ml). The organic layers arecombined and dried over anhydrous sodium sulfate. The solvent is removedunder reduced pressure and the resulting precipitate is triturated withpentane and filtered to afford the title compound as a white solid(0.082 g, 39%). Mass spectrum (m/z): 384.2 (M+1).

Preparation 43 Synthesis of methyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 15, Step A.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.70 g,4.093 mmol, see preparation 1) in CH₂Cl₂ (6 mL) at 0° C. are addedmethyl 4-amino-3,5-dimethylbenzoate (0.74 g, 4.093 mmol, see preparation12), and triethylamine (0.83 g, 8.187 mmol). After stirring the reactionmixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50%solution in ethyl acetate, 2.60 g, 8.187 mmol) is added via syringe andstirred at ambient temperature. After 12 hours, the solvent is removedunder reduced pressure and the residue is diluted with water andextracted with ethyl acetate. The organic layers are combined and driedover anhydrous Na₂SO₄, filtered, and concentrated under reducedpressure. The resulting residue is purified by flash chromatography(silica gel) using a gradient of 0-40% ethyl acetate in hexanes to givethe title compound as an off-white solid (1.10 g, 81%). Mass spectrum(m/z): 333.2 (M+1).

Preparation 44 Synthesis oftert-butyl-dimethyl-(3-piperidylmethoxy)silane

Scheme 15, Step B.

To a solution of piperidin-3-ylmethanol (2.10 g, 0.018 mol) in CH₂Cl₂(20 mL) is added triethylamine (5.53 g, 0.0547 mol) followed byt-butyldimethylchlorosilane (4.127 g, 0.0275 mol) and the reactionmixture is stirred at room temperature. After 24 hours, the reactionmixture is washed with water, saturated solution of NaHCO₃, and brine.The combined organic layers are dried over sodium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) over a gradient using 0-10% MeOH indichloromethane to afford the title compound (2.50 g, 60%). Massspectrum (m/z): 231.2 (M+1).

Preparation 45 Synthesis of methyl4-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 15, Step B.

To a solution of methyl4-(6-chloro-3-methylpicolinamido)-2,4-dimethylbenzoate (0.50 g, 0.0015mol), tert-butyl-dimethyl-(3-piperidylmethoxy)silane (0.42 g, 0.0018mol) and Cs₂CO₃ (1.96 g, 0.0060 mol) in 1,4-dioxane (20 ml) is addedPd₂(dba)₃ (0.14 g, 0.00015 mol) followed by S-Phos (0.062 g, 0.00015mol). The reaction mixture is purged with nitrogen for 5 minutes andthen heated at 80° C. After 24 hours, the reaction is cooled to ambienttemperature, filtered through Celite™, and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) to afford the title compound as awhite semi-solid (0.230 g, 30%). Mass spectrum (m/z): 526.5 (M+1).

Preparation 46 Synthesis of methyl4-[[6-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 15, Step C.

To a solution of methyl4-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(0.22 g, 0.873 mmol) in THF (3 ml) is added Bu₄NF 1.0 M in THF (2.00 ml)at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 8 hours, the reaction mixture is diluted withice-water and extracted twice with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 0-40% ethyl acetate inhexanes to afford the title compound as a white solid (0.06 g, 30%).Mass spectrum (m/z): 412.2 (M+1).

Example 11 Synthesis of4-[[6-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 15, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof methyl4-(6-(3-(hydroxymethyl)piperidin-1-yl)-3-methylpicolinamido)-3,5-dimethylbenzoate(0.06 g, 0.146 mmol) in THF:MeOH (4 ml:1 ml). After 12 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 3 with aqueous citricacid solution, and extracted with ethyl acetate (2×10 ml). The organiclayers are combined and dried over anhydrous sodium sulfate. The solventis removed under reduced pressure and the resulting precipitate istriturated with pentane and filtered to afford the title compound as anoff-white solid (0.03 g, 48%). Mass spectrum (m/z): 398.2 (M+1).

Preparation 47 Synthesis of methyl3-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 16, Step A.

To a solution of methyl3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoate(0.5 g, 0.0015 mol, see preparation 40),tert-butyl-dimethyl-(3-piperidylmethoxy)silane (0.41 g, 0.0018 mol, seepreparation 14) and Cs₂CO₃ (1.95 g, 0.006 mol) in 1,4-dioxane (20 ml) isadded Pd₂(dba)₃ (0.137 g, 0.00015 mol) followed by S-Phos (0.06 g,0.00015 mol). The reaction mixture is purged with nitrogen for 5 minutesand then heated at 80° C. After 24 hours, the reaction is cooled toambient temperature, filtered through Celite™, and washed with EtOAc.The combined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure and purified by flash chromatography(silica gel) using 20% EtOAc in hexane to afford the title compound as abrown semi-solid (0.2 g, 38%). Mass spectrum (m/z): 525.2 (M+1).

Preparation 48 Synthesis of methyl3-[[6-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 16, Step B.

To a solution of methyl3-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate(0.20 g, 0.38 mmol) in THF (4 ml) is added Bu₄NF 1.0 M in THF (1.5 ml)at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 8 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure. The resulting residue is purified by flashchromatography (neutral alumina) over a gradient using 50% ethyl acetatein hexane to afford the title compound as a white solid (0.18 g, 115%).Mass spectrum (m/z): 412.2 (M+1).

Example 12 Synthesis of3-[[6-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoicacid

Scheme 16, Step C.

A solution of aqueous 2N NaOH (3.00 ml) is added to a stirred solutionof methyl3-[[16-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate(0.18 g, 0.437 mmol) in THF (8 ml). After 12 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with citric acid,and extracted with ethyl acetate. The organic layers are combined anddried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting residue is purified by preparativeHPLC to afford the title compound as off white solid (57 mg, 14%). Massspectrum (m/z): 398.2 (M+1).

Preparation 49 Synthesis of ethyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 17, Step A.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (465 mg,2.71 mmol) in THF (5 ml), CH₂Cl₂ (5 ml) and DMF (0.01 ml, 129.33 μmoles)is added dropwise oxalyl chloride (0.3 ml, 3.46 mmoles) at 0° C. andreaction mixture is slowly allowed to warm to ambient temperature. After2 hours, the solvent is removed under reduced pressure and the residue.To the residue CH₂Cl₂ (20 ml) is added and reaction mixture is cooled to0° C., then ethyl 4-amino-3,5-dimethyl-benzoate (520 mg, 2.69 mmol) isadded followed by N,N-dimethylpyridin-4-amine (15 mg, 122.78 μmoles) andPyridine (0.66 ml, 8.16 mmoles). The cooling bath is removed and theclear yellow solution is allowed to warm to ambient temperature. After 1hour, the solvent is removed and the reaction mixture is diluted withethyl acetate and washed with 0.5N HCl, saturated solution of sodiumbicarbonate, and brine. The organic layers are combined and dried overanhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. Theresidue is purified by flash chromatography (silica gel) using 0-50%ethyl acetate in hexanes to give the title compound as a solid (790 mg,84%). Mass spectrum (m/z): 347.2 (M+1).

Preparation 50 Synthesis of ethyl4-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 17, Step B.

To a solution of ethyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate(275 mg, 792.93 μmoles), 4-methylpiperidin-4-ol (120 mg, 1.04 mmol) andCs₂CO₃ (0.8 g, 2.46 mmol) in 1,4-dioxane (6 ml) is added Pd(OAc)₂ (27mg, 120.26 μmoles) followed byracemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (54 mg, 86.72μmoles). The reaction mixture is purged with nitrogen for 5 minutes andthen heated to reflux. After 2 hours, the reaction is cooled to ambienttemperature and diluted with ammonium chloride and extracted twice withEtOAc. The combined organic layers are dried over sodium sulfate,filtered, and concentrated under reduced pressure. The resulting residueis purified by flash chromatography (silica gel) using 0-70% ethylacetate in hexane to afford the title compound as a yellow oil (0.27 g,80%). Mass spectrum (m/z): 426.2 (M+1).

Example 13 Synthesis of4-[[16-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 17, Step C.

A solution of aqueous 2N NaOH (5.00 ml) is added to a stirred solutionof ethyl4-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(0.27 g, 634.51 mmol) in THF:MeOH (10 ml:5 ml). After 1 hour at 50° C.,the organic solvent is removed under reduced pressure and the residue isdiluted with water, acidified to pH 6 with 5N HCl, and extracted withethyl acetate. The organic layers are combined with aqueous layer andconcentrated under reduced pressure. The solids are triturated withacetone/acetonitrile and filtered. The filtrate is dried over sodiumsulfate, filtered, and concentrated under reduced pressure to afford thetitle compound as an off-white solid (0.11 g, 43.6%). Mass spectrum(m/z): 398.2 (M+1).

Preparation 51 Synthesis of methyl3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoate

Scheme 18, Step A.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (465 mg,2.71 mmol) in THF (5 ml), CH₂Cl₂ (5 ml) and DMF (0.01 ml, 129.33 μmoles)is added dropwise oxalyl chloride (0.3 ml, 3.46 mmoles) at 0° C. and thereaction mixture is slowly allowed to warm to ambient temperature. After2 hours, the solvent is removed under reduced pressure. To the residueCH₂Cl₂ (20 ml) is added and reaction mixture is cooled to 0° C., thenmethyl 3-amino-3,5-dimethylbenzoate (490 mg, 2.73 mmol) is addedfollowed by N,N-dimethylpyridin-4-amine (15 mg, 122.78 μmoles) andpyridine (0.66 ml, 8.16 mmoles). The cooling bath is removed and theclear solution is allowed to warm to ambient temperature. After 1.5hours, the solvent is removed and the reaction mixture is diluted withethyl acetate and washed with 0.5N HCl, saturated solution of sodiumbicarbonate, and brine. The organic layers are combined and dried overanhydrous Na₂SO₄, filtered, and concentrated under reduced pressure togive the title compound as a light yellow solid (664 mg, 73%). Massspectrum (m/z): 333.2 (M+1).

Preparation 52 Synthesis of methyl3-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 18, Step B.

To a solution of methyl3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoate(315 mg, 946.55 μmoles), 4-methylpiperidin-4-ol (130 mg, 1.13 mmol) andCs₂CO₃ (0.9 g, 2.76 mmol) in 1,4-dioxane (7 ml) is added Pd(OAc)₂ (25mg, 89.93 μmoles) followed byracemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (56 mg, 89.93μmoles). The reaction mixture is purged with nitrogen for 5 minutes andthen heated to reflux. After 2 hours, the reaction is cooled to ambienttemperature and diluted with ammonium chloride and extracted with EtOAc.The combined organic layers are dried over sodium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) using 0-100% ethyl acetate inhexane to afford the title compound as a brown solid (0.27 g, 69%). Massspectrum (m/z): 412.2 (M+1).

Example 14 Synthesis of3-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoicacid

Scheme 18, Step C.

A solution of aqueous 2N NaOH (5.00 ml) is added to a stirred solutionof methyl3-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate(0.27 g, 656.13 mmol) in THF:MeOH (10 ml:5 ml). After 1 hour 50° C., theorganic solvent is removed under reduced pressure and the residue isdiluted with water, acidified to pH 6 with 5N HCl, and extracted withethyl acetate. The organic layers are combined and concentrated underreduced pressure. The solids are triturated with acetone/acetonitrileand filtered. The filtrate is dried over sodium sulfate, filtered andconcentrated under reduced pressure to afford the title compound as anoff-white solid (75 mg, 29%). Mass spectrum (m/z): 398.2 (M+1).

Preparation 53 Synthesis of methyl4-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]pyrrolidin-1-yl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 19, Step A.

To a solution of methyl4-(6-chloro-3-methylpicolinamido)-2,4-dimethylbenzoate (0.4 g, 1.2 mmol,see preparation 2), tert-butyl-dimethyl-(pyrrolidin-3-ylmethoxy)silane(0.775 g, 3.6 mmol) and Cs₂CO₃ (1.17 g, 3.6 mmol) in 1,4-dioxane (5 ml)is added Pd₂(dba)₃ (0.1 g, 0.12 mmol) followed by S-Phos (0.05 g, 0.12mmol). The reaction mixture is purged with nitrogen for 5 minutes andthen heated at 90° C. After 24 hours, the reaction is cooled to ambienttemperature, filtered through Celite™, and washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) using 10% ethyl acetate in hexanesto afford the title compound as a white semi-solid (1.2 g, crude). Massspectrum (m/z): 512.2 (M+1).

Preparation 54 Synthesis of methyl4-[[6-[3-(hydroxymethyl)pyrrolidin-1-yl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 19, Step B.

To a solution of methyl 4-[[6-[3-[[tert-butyl(dimethyl)silyl]oxymethyl]pyrrolidin-1-yl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(1.1 g, 2.15 mmol) in THF (7 ml) is added Bu₄NF 1.0 M in THF (5.00 ml)at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 6 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure. The resulting residue is purified by flashchromatography (silica gel) over a gradient using 0-50% ethyl acetate inhexanes to afford the title compound as an off-white solid (0.36 g,42%). Mass spectrum (m/z): 398.2 (M+1).

Example 15 Synthesis of4-[[6-[3-(hydroxymethyl)pyrrolidin-1-yl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 19, Step C.

A solution of NaOH (0.16 g) in H₂O (1 ml) is added to a stirred solutionof methyl4-[[6-[3-(hydroxymethyl)pyrrolidin-1-yl]-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(0.35 g, 0.88 mmol) in THF:MeOH (5 ml:1 ml). After 8 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 3 with aqueous citricacid solution, and extracted with ethyl acetate (2×10 ml). The organiclayers are combined and dried over anhydrous sodium sulfate. The solventis removed under reduced pressure and the resulting precipitate istriturated with diethyl ether and filtered to afford the title compoundas an off-white solid (73 mg, 33.7%). Mass spectrum (m/z): 384.2 (M+1).

Preparation 55 Synthesis of methyl4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 20, Step A.

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (6.00 g,0.03508 mol) in CH₂Cl₂ (50 ml) at 0° C. are added methyl4-amino-3,5-dimethylbenzoate (5.65 g, 0.03157 mol), andN,N-diisopropylethylamine (15.1 ml, 0.0877 mol). After stirring thereaction mixture for 10 minutes, 1-propanephosphonic acid cyclicanhydride (50% solution in ethyl acetate, 22.32 g, 0.07016 mol) is addedvia syringe and stirred at 60° C. After 3 hours, the solvent is removedunder reduced pressure and the residue is diluted with water andextracted with ethyl acetate. The organic layers are combined and driedover anhydrous Na₂SO₄, filtered, and concentrated under reducedpressure. The resulting residue is purified by flash chromatography(silica gel) using a gradient of 0-40% ethyl acetate in hexanes to givethe title compound as an off-white solid (8.70 g, 74%). Mass spectrum(m/z): 333.2 (M+1).

Preparation 56 Synthesis of methyl4-[[6-(4-methoxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 20, Step B.

To a solution of methyl4-(6-chloro-3-methylpicolinamido)-2,4-dimethylbenzoate (0.30 g, 0.90mmol), 4-methoxypiperidine (0.178 g, 1.8 mmol) and Cs₂CO₃ (0.88 g, 2.7mmol) in 1,4-dioxane (5 ml) is added Pd₂(dba)₃ (0.082 g, 0.09 mmol)followed by S-Phos (0.037 g, 0.09 mmol). The reaction mixture is purgedwith nitrogen for 5 minutes and then heated at 130° C. After 16 hours,the reaction is cooled to ambient temperature, filtered through Celite™,and washed with EtOAc. The combined filtrates are dried over sodiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) using20% ethyl acetate in hexane to afford the title compound as a lightyellow solid (0.14 g, 34%).

Example 16 Synthesis of4-[[6-(4-methoxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 20, Step C.

Lithium hydroxide (LiOH.H₂O, 0.026 g, 0.62 mmol) is added to a stirredsolution of methyl4-[[6-(4-methoxy-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(0.129 g, 0.313 mmol) in THF:H₂O:MeOH (0.7 ml:0.3 ml:0.7 ml). After 2hours at 50° C., the organic solvent is removed under reduced pressureand the residue is diluted with water, acidified to pH 6 with aqueous 1NHCl, and extracted with ethyl acetate (3×20 ml). The organic layers arecombined and dried over anhydrous sodium sulfate. The solvent is removedunder reduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as an off-whitesolid (0.11 g, 88%). Mass spectrum (m/z): 398.2 (M+1).

Preparation 57 Synthesis of methyl4-[[6-(4,4-difluoro-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 21, Step A.

To a solution of methyl4-(6-chloro-3-methylpicolinamido)-2,4-dimethylbenzoate (0.30 g, 0.90mmol, see preparation 43), 4,4-difluoropiperidine (0.283 g, 1.8 mmol)and Cs₂CO₃ (1.17 g, 3.6 mmol) in 1,4-dioxane (5 ml) is addedPdCl₂(dppf).CH₂Cl₂ (0.082 g, 0.0903 mmol) followed by S-Phos (0.037 g,0.0903 mmol). The reaction mixture is purged with nitrogen for 5 minutesand then heated at 130° C. After 16 hours, the reaction is cooled toambient temperature, filtered through Celite™, washed with EtOAc. Thecombined filtrates are dried over sodium sulfate, filtered, andconcentrated under reduced pressure to afford the title compound as alight yellow solid (0.240 g, 63%). Mass spectrum (m/z): 418.2 (M+1).

Example 17 Synthesis of4-[[6-(4,4-difluoro-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 21, Step B.

Lithium hydroxide (LiOH.H₂O, 0.048 g, 0.00115 mol) is added to a stirredsolution of methyl4-[[6-(4,4-difluoro-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-3,5-dimethyl-benzoate(0.24 g, 0.575 mmol) in THF:H₂O:MeOH (1.5 ml:0.7 ml:1.5 ml). After 3hours at 50° C., the organic solvent is removed under reduced pressureand the residue is diluted with water, acidified to pH 6 with aqueous 1NHCl, and extracted with ethyl acetate (3×20 ml). The organic layers arecombined and dried over anhydrous sodium sulfate. The solvent is removedunder reduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as a white solid(0.166 g, 71%). Mass spectrum (m/z): 404.2 (M+1).

Preparation 58 Synthesis of methyl4-[2-chloroquinoline-4-carbonyl)amino]-3,5-dimethyl-benzoate

Scheme 22, Step A.

To a solution of 2-chloroquinoline-4-carboxylic acid (5.00 g, 0.0024mol) in CH₂Cl₂ (50 mL) at 0° C. are added methyl4-amino-3,5-dimethylbenzoate (3.88 g, 0.02167 mol, see preparation 12)and N,N-diisopropylethylamine (12.5 ml, 0.07225 mol). After stirring thereaction mixture for 10 minutes, 1-propanephosphonic acid cyclicanhydride (50% solution in ethyl acetate, 31.0 ml, 0.048 mol) is addedvia syringe and heated at 40° C. After 5 hours, the reaction mixture isdiluted with water and extracted with dichloromethane. The organiclayers are combined and dried over magnesium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) using a gradient of 0-40% ethylacetate in hexanes. After purification the solid is triturated with 20%diethyl ether in pentane and dried to give the title compound as a whitesolid (8.50 g, 96%). Mass spectrum (m/z): 369.1 (M+1).

Preparation 59 Synthesis of methyl4-[[2-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]quinoline-4-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 22, Step B.

To a solution of methyl4-(2-chloroquinoline-4-carboxamido)-3,5-dimethylbenzoate, (0.50 g,0.00135 mol), tert-butyl-dimethyl-(4-piperidyloxy)silane (0.32 g, 0.0015mol, see preparation 3) and Cs₂CO₃ (1.77 g, 0.0054 mol) in 1,4-dioxane(5 ml) is added Pd₂(dba)₃ (0.124 g, 0.000135 mol) followed by S-Phos(0.060 g, 0.000135 mol). The reaction mixture is purged with nitrogenfor 5 minutes and then stirred at 80° C. After 4 hours, the reaction iscooled to ambient temperature, filtered through Celite™, and washed withEtOAc. The organic layers are combined and dried over sodium sulfate,filtered, and concentrated under reduced pressure to afford the titlecompound (0.21 g, 28%). Mass spectrum (m/z): 548.2 (M+1).

Preparation 60 Synthesis of methyl4-[[2-(4-hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-3,5-dimethyl-benzoate

Scheme 22, Step C.

To a solution of methyl4-(2-(4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)quinoline-4-carboxamido)-3,5-dimethylbenzoate(0.21 g, 0.00038 mol) in THF (4 ml) is added Bu₄NF 1.0 M in THF (4.0 ml)at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 14 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 0-40% ethyl acetate inhexanes to afford the title compound as a light yellow solid (0.13 g,78%). Mass spectrum (m/z): 434.2 (M+1).

Example 18 Synthesis of4-[[2-(4-hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-3,5-dimethyl-benzoicacid

Scheme 22, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof methyl4-(2-(4-hydroxypiperidin-1-yl)quinoline-4-carboxamido)-3,5-dimethylbenzoate(0.13 g, 0.0003 mol) in THF:MeOH (5 ml:2 ml). After 5 h at 50° C., theorganic solvent is removed under reduced pressure and the residue isdiluted with water acidified to pH 6 with aqueous 1N HCl and extractedwith ethyl acetate (2×20 ml). The organic layers are combined and driedover anhydrous sodium sulfate. The solvent is removed under reducedpressure and the resulting precipitate is triturated with pentane anddiethyl ether and filtered to afford the title compound as a lightyellow solid (0.05 g, 40%). Mass spectrum (m/z): 420.2 (M+1).

Preparation 61 Synthesis of methyl3-[(2-chloroquinoline-4-carbonyl)amino]-2,4-dimethyl-benzoate

Scheme 23, Step A.

To a solution of 2-chloroquinoline-4-carboxylic acid (0.40 g, 0.0019mol) in CH₂Cl₂ (8 mL) at 0° C. are added methyl3-amino-2,4-dimethylbenzoate (0.31 g, 0.0017 mol, see preparation 10)and triethylamine (0.80 ml, 0.0058 mol). After stirring the reactionmixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50%solution in ethyl acetate, 2.45 ml, 0.0038 mol) is added via syringe andstirred at room temperature. After 16 hours, the reaction is dilutedwith water and extracted twice with dichloromethane. The organic layersare combined and dried over magnesium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is trituratedwith 20% diethyl ether in pentane and filtered to give the titlecompound as an off-white solid (0.55 g, 77%). Mass spectrum (m/z): 369.1(M+1).

Preparation 62 Synthesis of methyl3-[[2-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 23, Step B.

To a solution of methyl3-(2-chloroquinoline-4-carboxamido)-2,4-dimethylbenzoate (0.54 g,0.00146 mol), tert-butyl-dimethyl-(4-piperidyloxy)silane (0.63 g,0.00293 mol, see preparation 3) and Cs₂CO₃ (1.43 g, 0.0044 mol) in1,4-dioxane (8 ml) is added Pd₂(dba)₃ (0.134 g, 0.000146 mol) followedby S-Phos (0.060 g, 0.000146 mol). The reaction mixture is purged withnitrogen for 5 minutes and then stirred at 80° C. After 16 hours, thereaction is cooled to ambient temperature, filtered through Celite™, andwashed with EtOAc. The organic layers are combined and dried over sodiumsulfate, filtered, and concentrated under reduced pressure to afford thetitle compound as a black semi-solid (1.31 g, 60%, crude). Mass spectrum(m/z): 548.2 (M+1).

Preparation 63 Synthesis of methyl3-[[2-(4-hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 23, Step C.

To a solution of methyl3-(2-(4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)quinoline-4-carboxamido)-2,4-dimethylbenzoate(1.30 g, 0.00087 mol) in THF (2.0 ml) is added Bu₄NF 1.0 M in THF (10.0ml) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 14 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) with ethyl acetate in hexanes to afford thetitle compound as a yellow solid (0.10 g, 27%). Mass spectrum (m/z):434.3 (M+1).

Example 19 Synthesis of3-[[2-(4-hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoicacid

Scheme 23, Step D.

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solutionof methyl3-(2-(4-hydroxypiperidin-1-yl)quinoline-4-carboxamido)-2,4-dimethylbenzoate(0.10 g, 0.00023 mol) in THF:MeOH (4 ml:2 ml). After 5 h at 50° C., theorganic solvent is removed under reduced pressure and the residue isdiluted with water, acidified to pH 6 with aqueous 1N HCl, and extractedwith ethyl acetate (2×20 ml). The organic layers are combined and driedover anhydrous sodium sulfate. The solvent is removed under reducedpressure and the resulting precipitate is triturated with pentane anddiethyl ether and filtered to afford the title compound as a lightyellow solid (0.03 g, 31%). Mass spectrum (m/z): 420.2 (M+1).

Preparation 64 Synthesis of methyl3-[(3-bromonaphthalene-1-carbonyl)amino]-2,4-dimethyl-benzoate

Scheme 24, Step A.

To a solution of 3-bromo-1-naphthoic acid (0.40 g, 1.59 mmol) in CH₂Cl₂(8 mL) at 0° C. are added methyl 3-amino-2,4-dimethylbenzoate (0.26 g,1.43 mmol, see preparation 10) and triethylamine (0.78 ml, 5.38 mmol).After stirring the reaction mixture for 10 minutes, 1-propanephosphonicacid cyclic anhydride (50% solution in ethyl acetate, 2.03 ml, 3.18mmol) is added via syringe and stirred at room temperature. After 16hours, the reaction is diluted with water and extracted with ethylacetate. The organic layers are combined and dried over magnesiumsulfate, filtered, and concentrated under reduced pressure. Theresulting residue is purified by flash chromatography (silica gel) with5% EtOAc in hexane as eluent to afford the product as a white solid(0.52 g, 79%). Mass spectrum (m/z): 412.3 (M+1).

Preparation 65 Synthesis of methyl3-[[3-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]naphthalene-1-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 24, Step B.

To a solution of methyl 3-(3-bromo-1-naphthamido)-2,4-dimethylbenzoate(0.48 g, 0.0011 mol), tert-butyl-dimethyl-(4-piperidyloxy)silane (0.75g, 0.0034 mol, see preparation 3) and Cs₂CO₃ (1.00 g, 0.0033 mol) in1,4-dioxane (8 ml) is added Pd₂(dba)₃ (0.10 g, 0.00011 mol) followed byS-Phos (0.045 g, 0.00011 mol). The reaction mixture is purged withnitrogen for 5 minutes and then stirred at 80° C. After 16 hours, thereaction is cooled to ambient temperature, filtered through Celite™ andwashed with EtOAc. The organic layers are combined and dried over sodiumsulfate, filtered, and concentrated under reduced pressure to afford thetitle compound as a black semi-solid (0.52 g, crude). Mass spectrum(m/z): 547.5 (M+1).

Preparation 66 Synthesis of methyl3-[[3-(4-hydroxy-1-piperidyl)naphthalene-1-carbonyl]amino]-2,4-dimethyl-benzoate

Scheme 24, Step C.

To a solution of methyl3-[[3-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]naphthalene-1-carbonyl]amino]-2,4-dimethyl-benzoate(0.30 g, 0.54 mmol) in THF (8.0 ml) is added Bu₄NF 1.0 M in THF (0.35 g,1.60 mmol) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 14 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) with ethyl acetate in hexanes to afford thetitle compound as a white solid (0.10 g, 55%). Mass spectrum (m/z):433.0 (M+1).

Example 20 Synthesis of3-[[3-(4-hydroxy-1-piperidyl)naphthalene-1-carbonyl]amino]-2,4-dimethyl-benzoicacid

Scheme 24, Step D.

A solution of aqueous 2N NaOH (3.00 ml) is added to a stirred solutionof methyl3-(3-(4-hydroxypiperidin-1-yl)-1-naphthamido)-2,4-dimethylbenzoate (0.10g, 0.23 mmol) in THF:MeOH (3 ml:1 ml). After 12 hours at roomtemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with aqueous 1N HCland extracted with dichloromethane (2×20 ml). The organic layers arecombined and dried over anhydrous sodium sulfate. The solvent is removedunder reduced pressure and the resulting precipitate is triturated withdiethyl ether and filtered to afford the title compound as a white solid(0.028 g, 29%). Mass spectrum (m/z): 419.2 (M+1).

Preparation 67 Synthesis of methyl3-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 25, Step A.

To a solution of 5-bromo-2-(trifluoromethyl)benzoic acid (1.0 g, 3.53mmol) in CH₂Cl₂ (6 ml) at room temperature are added methyl3-amino-3,5-dimethylbenzoate (0.44 g, 2.47 mmol, see preparation 12) andtrimethylamine (1.0 ml, 7.06 mmol). After stirring the reaction mixturefor 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solutionin ethyl acetate, 5.6 ml, 8.83 mmol) is added via syringe. After 14hours at ambient temperature, the reaction mixture is diluted withCH₂Cl₂, washed with water and brine. The organic layers are combined anddried over anhydrous Na₂SO₄, filtered, and concentrated under reducedpressure. The resulting residue is purified by flash chromatography(silica gel) using 20% ethyl acetate in hexanes to give the titlecompound as a white solid (0.6 g, 39%).

Preparation 68 Synthesis of methyl3-[[5-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 25, Step B.

To a solution of methyl3-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoate(0.20 g, 0.46 mmol), tert-butyl-dimethyl-(3-piperidylmethoxy)silane(0.11 g, 0.50 mmol, see preparation 3) and Cs₂CO₃ (0.45 g, 1.39 mmol) in1,4-dioxane (15 ml) is added Pd₂(dba)₃ (43 mg, 0.046 mmol) followed byS-Phos (19.3 mg, 0.046 m mol). The reaction mixture is purged withnitrogen for 5 minutes and then heated at 110° C. After 12 hours, thereaction is cooled to ambient temperature, filtered through Celite™, andwashed with EtOAc. The combined filtrates are dried over sodium sulfate,filtered, and concentrated under reduced pressure. The resulting residueis purified by flash chromatography (silica gel) using 30% ethyl acetatein hexane to afford the title compound as a brown semi-solid (180 mg,68%). Mass spectrum (m/z): 565.2 (M+1).

Preparation 69 Synthesis of methyl3-[[5-(4-hydroxy-1-piperidyl)-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoate

Scheme 25, Step C.

To a solution of methyl3-[[5-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoate(180 mg, 0.32 mmol) in THF (10.0 ml) is added Bu₄NF 1.0 M in THF (2.0ml) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 8 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (neutral alumina) over a gradient using 100% ethylacetate in hexane to afford the title compound as a white solid (0.11 g,76%). Mass spectrum (m/z): 451.2 (M+1).

Example 21 Synthesis of3-[[5-(4-hydroxy-1-piperidyl)-2-(trifluoromethyl)benzoyl]amino]-2,4-dimethyl-benzoicacid

Scheme 25, Step D.

A solution of aqueous 2N NaOH (2 ml) is added to a stirred solution ofmethyl3-[[6-[3-(hydroxymethyl)-1-piperidyl]-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate(0.11 g, 0.24 mmol) in THF (8 ml). After 12 hours at ambienttemperature, the organic solvent is removed under reduced pressure andthe residue is diluted with water, acidified to pH 4 with 1N HCl, andextracted twice with dichloromethane. The organic layers are combinedand dried over anhydrous sodium sulfate. The solvent is removed underreduced pressure and the resulting precipitate is triturated withpentane and diethyl ether and filtered to afford the title compound asan off-white solid (95 mg, 89%). Mass spectrum (m/z): 437.2 (M+1).

Preparation 70 Synthesis of methyl4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 26, Step A.

To a solution of 5-bromo-2-(trifluoromethyl)benzoic acid (1.00 g,0.00371 mol) in CH₂Cl₂ (15 mL) at room temperature are added methyl4-amino-3,5-dimethylbenzoate (0.46 g, 0.00260 mol, see preparation 12)and triethylamine (1.10 ml, 0.00743 mol). After stirring the reactionmixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50%solution in ethyl acetate, 6.00 ml, 0.00929 mol) is added via syringeand stirred at room temperature. After 14 hours, the reaction mixture isdiluted with water and extracted with dichloromethane. The organiclayers are combined and dried over magnesium sulfate, filtered, andconcentrated under reduced pressure. The resulting residue is purifiedby flash chromatography (silica gel) with 10-15% EtOAc to give the titlecompound as an off-white solid (0.45 g, 27.67%).

Mass spectrum (m/z): 430.0 (M+1).

Preparation 71 Synthesis of methyl4-[[5-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 26, Step B.

To a solution of methyl4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate(0.10 g, 232.44 μmol), tert-butyl-dimethyl-(4-piperidyloxy)silane (55.08mg, 255.68 mmol, see preparation 3) and Cs₂CO₃ (227.2 mg, 697.32 μmol)in 1,4-dioxane (2.5 ml) is added Pd₂(dba)₃ (21.28 mg, 23.24 μmol)followed by 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos)(9.54 mg, 23.24 μmol). The reaction mixture is purged with nitrogen for5 minutes and then heated at 120° C. After 8 hours, the reaction iscooled to ambient temperature, filtered through Celite™, and washed withEtOAc. The combined filtrates are dried over sodium sulfate, filtered,and concentrated under reduced pressure and purified by flashchromatography (neutral alumina) using of 15%-85% ethyl acetate inhexanes as eluent to afford the title compound as a pale yellow oil(0.10 g, 80%). Mass spectrum (m/z): 565.4 (M+1).

Preparation 72 Synthesis of methyl4-[[5-(4-hydroxy-1-piperidyl)-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate

Scheme 26, Step C.

To a solution of methyl4-[[5-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate(0.10 g, 177.08 μmoles) in THF (4 ml) is added Bu₄NF 1.0 M in THF (1.0ml) at 0° C. The reaction mixture is gradually warmed to ambienttemperature. After 6 hours, the reaction mixture is diluted withice-water and extracted with ethyl acetate. The organic layers arecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a residue. The residue is purified by flashchromatography (silica gel) over a gradient using 40-60% ethyl acetatein hexanes to afford the title compound as a light yellow solid (0.06 g,81.5%). Mass spectrum (m/z): 451.2 (M+1).

Example 22 Synthesis of4-[[5-(4-hydroxy-1-piperidyl)-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoicacid

Scheme 26, Step D.

A solution of aqueous 2N NaOH (1.5.00 ml) is added to a stirred solutionof methyl4-[[5-[4-[tert-butyl(dimethyl)silyl]oxy-1-piperidyl]-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate(60.0 mg, 133.20 μmoles) in THF:MeOH (5 ml:0.5 ml). After 12 h atambient temperature, the organic solvent is removed under reducedpressure and the residue is diluted with water, acidified to pH4 withaqueous citric acid, and extracted with ethyl acetate (2×20 ml). Theorganic layers are combined and dried over anhydrous sodium sulfate. Thesolvent is removed under reduced pressure and the resulting precipitateis triturated with pentane and diethyl ether filtered to afford thetitle compound as an off-white solid (0.04 g, 60%). Mass spectrum (m/z):437.2 (M+1).

In Vitro Binding to Human EP1, EP2, EP3 and EP4

hEP1 and hEP4 membranes are prepared from recombinant HEK293 cellsstably expressing human EP1 (Genbank accession number AY275470) or EP4(Genbank accession number AY429109) receptors. hEP2 and hEP3 membranesare prepared from HEK293 cells transiently transfected with EP2 (Genbankaccession number AY275471) or EP3 (isoform VI: Genbank accession numberAY429108) receptor plasmids. Frozen cell pellets are homogenized inhomogenization buffer using a Teflon/glass homogenizer. Membrane proteinis aliquoted and quick frozen on dry ice prior to storage at −80° C.Homogenization buffer contained 10 mM Tris-HCl, pH 7.4, 250 mM sucrose,1 mM EDTA, 0.3 mM indomethacin and plus Complete™, with EDTA, obtainedfrom Roche Molecular Biochemicals (Catalog Number 1 697 498).

Kd values for [3H]-PGE₂ binding to each receptor are determined bysaturation binding studies or homologous competition. Compounds aretested in a 96-well format using a three-fold dilution series togenerate a 10-point curve. Diluted compound is incubated with 20 μg/wellEP1, 10 μg/well EP2, 1 μg/well EP3 or 10 to 20 μg/well EP4 membrane for90 minutes at 25° C. in the presence of 0.3 to 0.5 nM [³H]-PGE₂(PerkinElmer, 118 to 180 Ci/mmol). The binding reaction is performed in200 μL MES buffer (10 mM MES pH 6.0 with KOH, 10 mM MgCl₂ and 1 mM EDTA)using 0.5 mL polystyrene 96-well deep-well plates. Nonspecific bindingis calculated by comparing binding in the presence and absence of 2 μMof PGE₂. The membranes are harvested by filtration (TomTek harvester),washed 4 times with cold buffer (10 mM MES pH 6.0 with KOH, 10 mMMgCl₂), dried in a 60° C. oven, and the radioactivity is quantified ascounts per minute (CPM) using a TopCount detector. Percent specificbinding is calculated as the percent of the binding in the absence ofany inhibitor, corrected for binding in the presence of 2 μM of PGE₂.Data are analyzed using a 4-parameter nonlinear logistic equation (ABaseEquation 205) as shown: y=(A+((B−A)/(1+((C/x)^D)))) where, y=% specificinhibition, A=bottom of the curve; B=top of the curve; C=relative IC₅₀concentration causing 50% inhibition based on the range of the data fromtop to bottom; D=Hill, Slope=slope of the curve. K_(i) conversion fromIC₅₀ Values (K_(i)=IC₅₀/(1+[L]/K_(d)) where [L] is the ligandconcentration). The compounds of Examples 1-22 herein are testedessentially as described above and exhibit a K_(i) value for hEP4 oflower than about 2 μM.

TABLE 2 In vitro binding of Example 1 to human EP1, EP2, EP3 and EP4Test hEP1, hEP2, hEP3, hEP4, Compound K_(i) (nM) K_(i) (nM) K_(i) (nM)K_(i) (nM) Example 1 >17500 >18900 >14000 76 ± 47 (n = 1) (n = 1) (n= 1) (n = 7)

Following the procedures essentially as described above, the data intable 2 demonstrate that the compound of Example 1 binds to hEP4 at lownanomolar concentrations. The data in table 2 also demonstrate thecompound of Example 1 binds to hEP4 more strongly than to hEP1, hEP2,and hEP3 indicating selectivity for the hEP4 receptor.

In Vitro Human EP4 Functional Antagonist Activity

Assays are conducted in recombinant HEK293 cells stably expressing humanEP4 receptor. The cell lines are maintained by culturing in DMEM withhigh glucose and pyridoxine hydrochloride (Invitrogen) supplemented with10% fetal bovine serum (FBS), 1 mM sodium pyruvate, 10 mM HEPES, 500μg/ml geneticin and 2 mM L-glutamine. Confluent cultures are grown at37° C. in an atmosphere containing 5% CO₂. Cells are harvested using2.5% Trypsin-EDTA, suspended in freeze media (FBS with 6% DMSO) at 10⁷cells/mL and aliquots are stored in liquid nitrogen. Just before assay,cells are thawed in DMEM, centrifuged, and resuspended in cAMP buffer.

The inhibition of PGE₂-stimulated cAMP production by EP4 antagonists ismeasured using HTRF; (Cisbio catalog #62AM4PEB). An aliquot equivalentto 4000 cells is incubated with 50 μL cAMP assay buffer containing EC₈₀of PGE₂ (0.188 nM PGE₂ from Sigma, catalog #P5640-10 mg) and antagonistsat room temperature for 20 minutes. cAMP assay buffer contains 500 mLHBSS (Hank's Balanced Salt Solution), 0.1% BSA, 20 mM HEPES and 200 μMIBMX (Sigma I5879). CJ-042794(4-{(1S)-1[({5-chloro-2-[(4-fluorophenyl)oxy]phenyl}carbonyl)amino]ethyl}benzoicacid) serves as a positive control. To measure the cAMP levels, cAMP-d2conjugate and anti cAMP-cryptate conjugate in lysis buffer are incubatedwith the treated cells at room temperature for 1 hour. The HTRF signalis detected using an EnVision® plate reader (Perkin-Elmer) to calculatethe ratio of fluorescence at 665 nm to 620 nm. The raw data areconverted to cAMP amount (pmole/well) using a cAMP standard curvegenerated for each experiment. Data are analyzed using a 4-parameternonlinear logistic equation (ABase Equation 205) as shown:y=(A+((B−A)/(1+((C/x)^D)))) where, y=% specific inhibition, A=Bottom ofthe curve, B=Top of the curve, C=Relative IC₅₀=concentration causing 50%inhibition based on the range of the data from top to bottom, D=Hill,Slope=slope of the curve.

Following the procedures essentially as described above, the compound ofExample 1 has an IC₅₀ of 5.6±2.8 nM (n=8) measured at human EP4. Thisdemonstrates that the compound of Example 1 is a potent antagonist ofhuman EP4 in vitro.

In Vitro Rat EP4 Functional Antagonist Activity

Rat EP4 cDNA (Genebank Accession# NM_(—)03276) is cloned into pcDNA 3.1vector and subsequently transfected in HEK293 cells for receptorexpression. Rat EP4 stable clone is scaled up and then frozen down ascell bank for future compounds screening. To test EP4 antagonistcompounds in rEP4 cells, thaw the frozen cells and then resuspend cellsin cAMP assay buffer. The cAMP buffer is made by HBSS without Phenol Red(Hyclone, SH30268) supplemented with 20 mM HEPES (Hyclone, SH30237),0.1% BSA (Gibco, 15260) and 125 μM IBMX (Sigma, 15879). The cells areplated into 96-well half area flat-bottom polystyrene black plates(Costar 3694). Compounds are serial diluted with DMSO to give 10-pointconcentration response curves. Then diluted compounds are added intocAMP assay buffer which contains PGE₂ (Cayman 14010, in a concentrationpredetermined to produce an EC₈₀) at ratio of DMSO/buffer at 1/100. Thecells are treated with compounds in the presence of PGE₂ (EC₈₀concentration) for 30 minutes at room temperature. The cAMP levelsgenerated from the cells are quantified by a cAMP HTRF assay kit (Cisbio62AM4PEC). The plates are read on an EnVision plate reader using HTRFoptimized protocol (PerkinElmer). IC₅₀'s are calculated using GraphpadPrism (v. 4) nonlinear regression, sigmoidal dose response curvefitting.

Following the procedures essentially as described above, the compound ofExample 1 has an IC₅₀ of 12 nM measured at rat EP4. This demonstratesthat the compound of Example 1 is a potent antagonist of rat EP4 invitro.

In Vitro Antagonist Activity in Human Whole Blood

The inhibitory effects of PGE₂ on LPS-induced TNFα production frommacrophages/monocytes are believed to be mediated by EP4 receptors (SeeMurase, A., et al., Life Sciences, 82:226-232 (2008)). The ability ofthe compound of Example 1 to reverse the inhibitory effect of PGE₂ onLPS-induced TNFα production in human whole blood is an indicia offunctional activity.

Blood is collected from normal volunteer donors into sodium heparinvacutainer tubes. Donors have not taken NSAIDs or celecoxib within 48hours or glucocorticoids within two weeks of the donation. Alltubes/donor are pooled into 50 mL Falcon conical centrifuge tubes and 98μL/well is distributed into 96-well tissue culture plates (Falcon 3072).Compounds are diluted into DMSO to 100× final and 1 μL/well intriplicate is added to the blood to give 7 point concentration responsecurves. The blood is pretreated with the compounds at 37° C., in a 5%CO₂ humidified atmosphere, for 30 minutes, after which 1 μL/well of asolution of 1 mg/mL of lipopolysaccharide (LPS) (Sigma 0111:B4) in 0.2mg/mL bovine serum albumin (BSA)/PBS+/−1 mM PGE₂ (Cayman 14010) is addedto give a final LPS concentration of 10 μg/mL+/−10 nM PGE₂. The platesare incubated for 20-24 hours at 37° C. in a 5% CO₂ humidifiedatmosphere. The plates are centrifuged at 1800×g, 10 minutes at 22° C.,in an Eppendorf 5810R centrifuge. Plasma is removed from the cell layerand is transferred to v-bottom polypropylene plates. TNFα levels in 2 μLplasma are quantified by a commercially available enzyme immunoassay(R&D Systems DY210), using Immulon 4 HBX plates (Thermo 3855) and3,3′,5,5′ tetramethylbiphenyl-4,4′-diamine substrate (KPL 50-76-03). Theplates are read at A₄₅₀-A₆₅₀ on a plate reader (Molecular DevicesVersamax) using SOFTmaxPRO (v. 4.3.1) software. IC₅₀s are calculatedusing Graphpad Prism (v. 4) nonlinear regression, sigmoidal doseresponse curve fitting. Results are expressed as the geometricmean±standard deviation; n=number of independent determinations.

Following the procedures essentially as described above, the compound ofExample 1 has an IC₅₀ of 123±81 nM (n=8) measured at human EP4. Thisdemonstrates that the compound of Example 1 is a potent EP4 antagonistin the human blood TNFα induction assay.

We claim:
 1. A pharmaceutical composition comprising a compound whichis:

or a pharmaceutically acceptable salt thereof, in combination with oneor more pharmaceutically acceptable carriers, diluents, or excipients.2. The pharmaceutical composition according to claim 1 wherein thecompound is:


3. The pharmaceutical composition according to claim 2 wherein thecompound is hydrated.
 4. The pharmaceutical composition according toclaim 3 wherein the hydrated compound is characterized by a substantialpeak in the X-ray diffraction spectrum, at diffraction angle 2-theta, of9.0°, in combination with two or more peaks at diffraction angle 2-thetaselected from the group consisting of 5.8°, 8.5°, 9.8°, 11.6°, 11.8°,17.5°, and 24.2°.